- Unexpected formation of new bicyclic γ-lactams by dimerization of α-chloroacetoacetanilidesHan, Minsoo; Nam, Kee-Dal; Hahn, Hoh-Gyu; Shin, Dongyun, Tetrahedron Letters, 2008, 49(35), 5217-5219
Cas no 97-36-9 (2,4-Dimethylacetoacetanilide)
2,4-Dimethylacetoacetanilide structure
Product Name:2,4-Dimethylacetoacetanilide
CAS No:97-36-9
MF:C12H15NO2
MW:205.253003358841
MDL:MFCD00039836
CID:34899
PubChem ID:222464
Update Time:2024-10-25
2,4-Dimethylacetoacetanilide Chemical and Physical Properties
Names and Identifiers
-
- N-(2,4-Dimethylphenyl)-3-oxobutanamide
- AAMX
- 2',4'-dimethylacetoacetanilide
- acetoacet-m-xylidide
- n-(2,4-dimethylphenyl)-3-oxobutyramide
- 2',4'-Acetoacetoxylidide
- 2,4-Dimethylacetoacetanilide
- ',4'-Dimethylacetoacetanilide
- 4'-Dimethylacetoacetanilide
- 2-Dicyclohexylphosphino-2'-(N,N-diMethylaMino)biphenyl
- AAM
- Acetoaceto-m-xylidide
- Acetoacetyl-m-xylidide
- 2,4-Acetoacetxylidide
- 2,4-Acetoacetoxylidide
- Butanamide, N-(2,4-dimethylphenyl)-3-oxo-
- Acetoacetic acid m-xylidide
- N-Acetoacetyl-2,4-xylidine
- 1-Acetoacetylamino-2,4-dimethylbenzene
- m-Acetoacetoxylidide
- Acetoacet-2,4-dimethylphenyl
- Acetoacetanilide, 2',4'-dimethyl-
- 3-Oxo-N-(2,4-methylphenyl)butanamide
- 84GV
- 2′,4′-Acetoacetoxylidide (6CI, 7CI, 8CI)
- N-(2,4-Dimethylphenyl)-3-oxobutanamide (ACI)
- 2′,4′-Dimethylacetoacetanilide
- N-(2,4-Dimethylphenyl)acetoacetamide
- NSC 8398
- o,p-Dimethylacetoacetanilide
- EN300-18246
- 84GV04HEUG
- Butanamide, N-(2,4,-dimethylphenyl)-3-oxo
- CAS-97-36-9
- NCGC00164201-01
- CS-0067139
- N-(2,4-dimethylphenyl)-3-oxo-butyric acid amide
- UNII-84GV04HEUG
- Q27269525
- NS00009606
- E77599
- N-(2,4-Dimethylphenyl)-3-oxobutanamide #
- F0001-2304
- SCHEMBL295936
- W-100110
- DTXSID4040719
- EC 202-576-0
- N-Acetoacetyl-2,4-xilidide
- Butanamide,4-dimethylphenyl)-3-oxo-
- m-Acetoaceto-Xylidide
- STK301606
- AKOS000120893
- DTXCID2020719
- N-Acetoacetyl-2,4-xylidine 100 microg/mL in Acetonitrile
- NSC-8398
- BS-4159
- 3-12-00-02484 (Beilstein Handbook Reference)
- BRN 2110911
- N-ACETOACETYL-M-XYLIDIN
- 97-36-9
- MFCD00039836
- NCGC00255500-01
- EINECS 202-576-0
- Tox21_302083
- N-(2,4-Dimethylphenyl)-3-oxobutyramide, 99.5%
- CHEMBL1877137
- N-(24-Dimethylphenyl)-3-oxobutyramide
- NSC8398
-
- MDL: MFCD00039836
- Inchi: 1S/C12H15NO2/c1-8-4-5-11(9(2)6-8)13-12(15)7-10(3)14/h4-6H,7H2,1-3H3,(H,13,15)
- InChI Key: HGVIAKXYAZRSEG-UHFFFAOYSA-N
- SMILES: O=C(CC(C)=O)NC1C(C)=CC(C)=CC=1
Computed Properties
- Exact Mass: 205.11000
- Monoisotopic Mass: 205.11
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 15
- Rotatable Bond Count: 3
- Complexity: 250
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Surface Charge: 0
- Tautomer Count: 8
- XLogP3: 1.9
- Topological Polar Surface Area: 46.2
Experimental Properties
- Color/Form: White crystalline powder.
- Density: 1.24
- Melting Point: 88-91 oC
- Boiling Point: 343.93°C (rough estimate)
- Flash Point: 171?°C
- Refractive Index: 1.5160 (estimate)
- PSA: 46.17000
- LogP: 2.29400
- Solubility: Not determined
2,4-Dimethylacetoacetanilide Security Information
-
Symbol:
- Signal Word:Warning
- Hazard Statement: H302,H319
- Warning Statement: P305+P351+P338
- WGK Germany:1
- Hazard Category Code: R22: harmful if swallowed.
- Safety Instruction: S24/25
- RTECS:AK4585000
-
Hazardous Material Identification:
- Risk Phrases:R22
- Storage Condition:Store at room temperature
2,4-Dimethylacetoacetanilide Customs Data
- HS CODE:2924299090
- Customs Data:
China Customs Code:
2924299090Overview:
2924299090. Other cyclic amides(Including cyclic carbamates)(Including their derivatives as well as their salts). VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%
Declaration elements:
Product Name, component content, use to, packing
Summary:
2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%
2,4-Dimethylacetoacetanilide Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | D101375-25g |
2,4-Dimethylacetoacetanilide |
97-36-9 | 99% | 25g |
¥29.90 | 2023-09-03 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | D101375-1kg |
2,4-Dimethylacetoacetanilide |
97-36-9 | 99% | 1kg |
¥230.90 | 2023-09-03 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | D101375-100g |
2,4-Dimethylacetoacetanilide |
97-36-9 | 99% | 100g |
¥55.90 | 2023-09-03 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | D101375-250g |
2,4-Dimethylacetoacetanilide |
97-36-9 | 99% | 250g |
¥87.90 | 2023-09-03 | |
| SHANG HAI YI EN HUA XUE JI SHU Co., Ltd. | R012155-250g |
2,4-Dimethylacetoacetanilide |
97-36-9 | 99% | 250g |
¥82 | 2024-07-19 | |
| SHANG HAI YI EN HUA XUE JI SHU Co., Ltd. | R012155-1kg |
2,4-Dimethylacetoacetanilide |
97-36-9 | 99% | 1kg |
¥219 | 2024-07-19 | |
| TRC | D481205-5g |
N-(2,4-Dimethylphenyl)-3-oxobutanamide |
97-36-9 | 5g |
$ 129.00 | 2023-09-07 | ||
| TRC | D481205-10g |
N-(2,4-Dimethylphenyl)-3-oxobutanamide |
97-36-9 | 10g |
$219.00 | 2023-05-18 | ||
| TRC | D481205-25g |
N-(2,4-Dimethylphenyl)-3-oxobutanamide |
97-36-9 | 25g |
$ 380.00 | 2022-06-05 | ||
| TRC | D481205-50g |
N-(2,4-Dimethylphenyl)-3-oxobutanamide |
97-36-9 | 50g |
$821.00 | 2023-05-18 |
2,4-Dimethylacetoacetanilide Production Method
Production Method 1
Production Method 2
Production Method 3
Reaction Conditions
1.1 Catalysts: Sodium hydroxide Solvents: Toluene , Water ; 12 h, reflux
Reference
- An efficient synthesis, characterization, and antimicrobial screening of tetrahydropyrimidine derivativesGodhani, Dinesh R.; Dobariya, Purvesh B.; Jogel, Anand A.; Sanghani, Anil M.; Mehta, Jignasu P., Medicinal Chemistry Research, 2014, 23(5), 2417-2425
Production Method 4
Production Method 5
Production Method 6
Reaction Conditions
1.1 Solvents: Water ; reflux
Reference
- Method for the continuous production of acetoacetic acid arylamides via the addition reaction of optionally substituted primary and secondary aryl amines with diketene in the presence of water and using reactive distillation, World Intellectual Property Organization, , ,
Production Method 7
Reaction Conditions
Reference
- Process for preparation of polysubstituted 4H-pyran compounds, China, , ,
Production Method 8
Production Method 9
Reaction Conditions
1.1 Reagents: Potassium hydroxide Catalysts: Titania Solvents: 1H-Imidazolium, 1-methyl-3-nitro-, salt with trinitromethane (1:1) ; 4 h, 90 °C
Reference
- TiO2 nanoparticles supported synthesis of acetoacetanilide derivatives in green mediaGoswami, P. G.; Dhadda, S.; Yadav, K.; Jangid, D. K.; Guleria, A.; et al, Research Journal of Chemistry and Environment, 2021, 25(5), 127-134
Production Method 10
Reaction Conditions
1.1 Catalysts: Sodium hydroxide Solvents: Toluene ; 15 h, 120 °C
Reference
- Synthesis, characterization, crystal and molecular structure analysis of N-(2,4-dimethylphenyl)-6-methyl-4-(3-nitrophenyl)-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxamideNaveen, S.; Adlakha, Priti; Dholakia, Chintan; Shah, Anamik; Sridhar, M. A.; et al, Structural Chemistry, 2006, 17(6), 569-575
Production Method 11
Reaction Conditions
1.1 Catalysts: Triethylamine Solvents: Benzene ; 4 h, reflux
Reference
- Synthesis and biological evaluation of 3-acyl-2-phenylamino-1,4-dihydroquinolin-4(1H)-one derivatives as potential MERS-CoV inhibitorsYoon, Ji Hye; Lee, Jun Young; Lee, Jihye; Shin, Young Sup; Jeon, Sangeun; et al, Bioorganic & Medicinal Chemistry Letters, 2019, 29(23),
Production Method 12
Reaction Conditions
1.1 Catalysts: Sodium hydroxide , Water Solvents: Toluene ; 24 h, reflux
Reference
- Synthesis, characterization, anti bacterial and antifungal activity of some novel pyrazole derivativeShah, Nilay; Karia, Denish C., Chemistry & Biology Interface, 2018, 8(5), 284-293
Production Method 13
Reaction Conditions
1.1 Catalysts: Sodium hydroxide Solvents: Toluene ; 4 - 10 h, 110 °C
Reference
- Synthesis and characterization of esters and amides of 3-arylaminobut-2-enoic acid via solvent-free condensationLu, Yun; Cui, Liang; Sun, Zhi-ming; Lei, Jun-yu; Yi, Jian-jun; et al, Huaxue Shiji, 2019, 41(3), 274-282
Production Method 14
Reaction Conditions
1.1 Catalysts: Potassium hydroxide Solvents: Toluene ; 24 h, reflux
Reference
- Synthesis of thiazolo[3,2-a]pyrimidine molecules, in-vitro cytotoxic evaluation and molecular docking studiesJadeja, Jaysinh; Savant, Mahesh, Journal of the Iranian Chemical Society, 2023, 20(7), 1491-1502
Production Method 15
Reaction Conditions
1.1 Catalysts: 1-Butyl-3-methylimidazolium hydroxide Solvents: Xylene ; heated
Reference
- Study on reaction of substituted 4-methylquinolin-2(1H)-ones with sodium azideDuan, Le The; Thanh, Nguyen Dinh; Nguyet, Nguyen Thi Minh; Hoai, Le Thi; Ha, Nguyen Thi Thu, International Electronic Conference on Synthetic Organic Chemistry, 2017, (2017), 1-6
Production Method 16
Reaction Conditions
1.1 Reagents: Potassium hydroxide Solvents: Toluene ; 8 h, reflux
Reference
- Phenothiazine and amide-ornamented novel nitrogen heterocyclic hybrids: synthesis, biological and molecular docking studiesSivaramakarthikeyan, Ramar; Karuppasamy, Ayyanar; Iniyaval, Shunmugam; Padmavathy, Krishnaraj; Lim, Wei-Meng; et al, New Journal of Chemistry, 2020, 44(10), 4049-4060
Production Method 17
Reaction Conditions
1.1 Reagents: Potassium hydroxide Solvents: Toluene ; 8 h, rt → reflux
Reference
- Phenothiazine and amide-ornamented dihydropyridines via a molecular hybridization approach: design, synthesis, biological evaluation and molecular docking studiesSivaramakarthikeyan, Ramar; Iniyaval, Shunmugam; Padmavathy, Krishnaraj; Liew, Hui-Shan; Looi, Chin-King; et al, New Journal of Chemistry, 2019, 43(43), 17046-17057
Production Method 18
Production Method 19
Production Method 20
Reaction Conditions
1.1 Catalysts: Sodium hydroxide Solvents: Toluene ; 10 - 15 h, 110 °C
Reference
- Synthesis, screening for antitubercular activity and 3D-QSAR studies of substituted N-phenyl-6-methyl-2-oxo-4-phenyl-1,2,3,4-tetrahydropyrimidine-5-carboxamidesVirsodia, Vijay; Pissurlenkar, Raghuvir R. S.; Manvar, Dinesh; Dholakia, Chintan; Adlakha, Priti; et al, European Journal of Medicinal Chemistry, 2008, 43(10), 2103-2115
2,4-Dimethylacetoacetanilide Raw materials
2,4-Dimethylacetoacetanilide Preparation Products
2,4-Dimethylacetoacetanilide Suppliers
Suzhou Senfeida Chemical Co., Ltd
Gold Member
(CAS:97-36-9)2',4'-Dimethylacetoacetanilide
Order Number:sfd11520;1619333
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Quantity:200kg/Company Customization
Purity:99.9%/98%
Pricing Information Last Updated:Friday, 19 July 2024 14:35
Price ($):discuss personally
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Tiancheng Chemical (Jiangsu) Co., Ltd
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(CAS:97-36-9)2,4-二甲基-N-乙酰乙酰苯胺
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Quantity:25KG,200KG,1000KG
Purity:99%
Pricing Information Last Updated:Friday, 20 June 2025 12:29
Price ($):discuss personally
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2,4-Dimethylacetoacetanilide Related Literature
-
Yiding Jiao,Liqun Kang,Jasper Berry-Gair,Kit McColl,Jianwei Li,Haobo Dong,Hao Jiang,Ryan Wang,Furio Corà,Dan J. L. Brett,Ivan P. Parkin J. Mater. Chem. A, 2020,8, 22075-22082
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Albertus D. Handoko,Khoong Hong Khoo,Teck Leong Tan,Hongmei Jin,Zhi Wei Seh J. Mater. Chem. A, 2018,6, 21885-21890
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Jing Yu,Yu-Qi Lyu,Jiapeng Liu,Mohammed B. Effat,Junxiong Wu J. Mater. Chem. A, 2019,7, 17995-18002
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J. Zagora,M. Vosla?,L. Schreiberová,I. Schreiber Phys. Chem. Chem. Phys., 2002,4, 1284-1291
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Zhixia Liu,Tingjian Chen,Floyd E. Romesberg Chem. Sci., 2017,8, 8179-8182
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Recommended suppliers
Suzhou Senfeida Chemical Co., Ltd
(CAS:97-36-9)2',4'-Dimethylacetoacetanilide
Purity:99.9%/98%
Quantity:200kg/Company Customization
Price ($):Inquiry/Inquiry
Tiancheng Chemical (Jiangsu) Co., Ltd
(CAS:97-36-9)2,4-二甲基-N-乙酰乙酰苯胺
Purity:99%
Quantity:25KG,200KG,1000KG
Price ($):Inquiry