Cas no 870997-57-2 (2-Amino-N,3-dimethylbenzamide)

2-Amino-N,3-dimethylbenzamide structure
2-Amino-N,3-dimethylbenzamide structure
Product Name:2-Amino-N,3-dimethylbenzamide
CAS No:870997-57-2
MF:C9H12N2O
MW:164.204381942749
CID:1028197
PubChem ID:16770689
Update Time:2024-10-26

2-Amino-N,3-dimethylbenzamide Chemical and Physical Properties

Names and Identifiers

    • 2-Amino-N,3-dimethylbenzamide
    • 2-amino-3,N-dimethyl benzamide
    • 2-Amino-3-methyl-N-methylbenzamide
    • 2-amino-N,3-dimethylbenzamide(SALTDATA: FREE)
    • 2-azanyl-N,3-dimethyl-benzamide
    • Methyl 2-amino-3-methylbenzoate
    • 2-Amino-N,3-dimethylbenzamide (ACI)
    • 2-Amino-3,N-dimethyl-benzamide
    • AKOS000127207
    • FBOWFVWOCBTBPH-UHFFFAOYSA-N
    • MFCD09042975
    • STL182345
    • BCP30913
    • DTXSID70588163
    • Z135505264
    • 2-Amino-3-methyl-N-methylbenzamide;
    • DTXCID30538927
    • BS-36085
    • EN300-1264115
    • F87524
    • CS-0232154
    • SCHEMBL635088
    • 870997-57-2
    • MDL： MFCD09042975
    • Inchi： 1S/C9H12N2O/c1-6-4-3-5-7(8(6)10)9(12)11-2/h3-5H,10H2,1-2H3,(H,11,12)
    • InChI Key： FBOWFVWOCBTBPH-UHFFFAOYSA-N
    • SMILES： O=C(C1C(N)=C(C)C=CC=1)NC

Computed Properties

  • Exact Mass: 164.09500
  • Monoisotopic Mass: 164.094963011g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 2
  • Complexity: 170
  • 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
  • XLogP3: 1.4
  • Topological Polar Surface Area: 55.1?2

Experimental Properties

  • PSA: 55.12000
  • LogP: 1.90890

2-Amino-N,3-dimethylbenzamide Customs Data

  • HS CODE：2924299090
  • Customs Data：

    China Customs Code:

    2924299090

    Overview:

    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-Amino-N,3-dimethylbenzamide Pricemore >>

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2-Amino-N,3-dimethylbenzamide Production Method

Production Method 1

Reaction Conditions
1.1 Solvents: Water ;  30 min, 35 °C
1.2 Reagents: Acetic acid Solvents: Ethyl acetate ;  1 h, 36 °C
1.3 Reagents: Methylamine Solvents: Water ;  2.5 h, 36 °C
Reference
Synthesis of 2-amino-N, 3-dimethyl-5-thiocyanatobenzamide
Sun, Bin, Huaxue Yanjiu Yu Yingyong, 2015, 27(11), 1746-1750

Production Method 2

Reaction Conditions
1.1 Catalysts: Pyridine Solvents: Ethyl acetate ;  2 h, 50 - 60 °C
2.1 Reagents: Acetic acid Solvents: Water ;  rt → 30 °C; 20 min, 30 °C
Reference
An improved synthesis of 2-amino-5-chloro-N,3-dimethylbenzamide
Liu, Jian-hua; et al, Nongyao, 2013, 52(11), 793-795

Production Method 3

Reaction Conditions
1.1 Reagents: Triethylamine ,  Ethyl chloroformate Solvents: Tetrahydrofuran ;  10 °C
1.2 Solvents: Tetrahydrofuran
2.1 Reagents: Hydrogen Catalysts: Palladium Solvents: Ethanol
Reference
Insecticidal anthranilic diamides: A new class of potent ryanodine receptor activators
Lahm, George P.; et al, Bioorganic & Medicinal Chemistry Letters, 2005, 15(22), 4898-4906

Production Method 4

Reaction Conditions
1.1 Reagents: Sodium hydroxide Catalysts: Carbon ,  Ferric chloride hexahydrate Solvents: Water ;  20 °C → 70 °C
1.2 Reagents: Hydrazine hydrate (1:1) ;  70 °C; 70 °C
1.3 Reagents: Sulfuric acid Solvents: Water ;  pH 7, rt; 1 h, rt
2.1 Catalysts: Pyridine Solvents: Acetonitrile ;  rt → 60 °C
2.2 Reagents: Phosgene Solvents: Acetonitrile ;  1.5 h, 50 - 60 °C; 4 h, 50 - 60 °C; 60 °C → reflux; reflux → rt
2.3 Reagents: Acetic acid Solvents: Water ;  30 min, reflux; 1 h, reflux; reflux → rt
2.4 Reagents: Water
Reference
Synthesis of 2-amino-5-chloro-N,3-dimethylbenzamide
Zhang, Ting; et al, Jingxi Huagong Zhongjianti, 2010, 40(5), 17-19

Production Method 5

Reaction Conditions
1.1 Reagents: 1,1′-Carbonyldiimidazole Solvents: Dimethylformamide ;  1 - 24 h, 40 °C
1.2 0.5 - 12 h, rt
Reference
Development of novel 2-[4-(aminoalkoxy)phenyl]-4(3H)-quinazolinone derivatives as potent and selective histamine H3 receptor inverse agonists
Mizutani, Takashi; et al, Bioorganic & Medicinal Chemistry Letters, 2008, 18(23), 6041-6045

Production Method 6

Reaction Conditions
1.1 Reagents: Hydrogen Catalysts: Palladium Solvents: Ethanol
Reference
Insecticidal anthranilic diamides: A new class of potent ryanodine receptor activators
Lahm, George P.; et al, Bioorganic & Medicinal Chemistry Letters, 2005, 15(22), 4898-4906

Production Method 7

Reaction Conditions
1.1 Reagents: Acetic acid Solvents: Water ;  rt → 30 °C; 20 min, 30 °C
Reference
An improved synthesis of 2-amino-5-chloro-N,3-dimethylbenzamide
Liu, Jian-hua; et al, Nongyao, 2013, 52(11), 793-795

Production Method 8

Reaction Conditions
1.1 Reagents: Thionyl chloride Solvents: Toluene ;  70 °C
1.2 Solvents: Ethanol ,  Dichloromethane ;  -15 °C; overnight, -15 °C
Reference
Synthesis process of 2-amino-5-cyano-N, 3-dimethyl-benzamide intermediate of cyantraniliprole insecticide
Sun, Bin; et al, Huaxue Yanjiu Yu Yingyong, 2013, 25(4), 599-603

Production Method 9

Reaction Conditions
1.1 Solvents: 1,4-Dioxane ;  rt; overnight, rt
2.1 Solvents: Water ;  30 min, 35 °C
2.2 Reagents: Acetic acid Solvents: Ethyl acetate ;  1 h, 36 °C
2.3 Reagents: Methylamine Solvents: Water ;  2.5 h, 36 °C
Reference
Synthesis of 2-amino-N, 3-dimethyl-5-thiocyanatobenzamide
Sun, Bin, Huaxue Yanjiu Yu Yingyong, 2015, 27(11), 1746-1750

Production Method 10

Reaction Conditions
1.1 Reagents: Hydrogen Catalysts: Palladium Solvents: Methanol ;  3 h, 1 MPa
2.1 Catalysts: Pyridine Solvents: Ethyl acetate ;  2 h, 50 - 60 °C
3.1 Reagents: Acetic acid Solvents: Water ;  rt → 30 °C; 20 min, 30 °C
Reference
An improved synthesis of 2-amino-5-chloro-N,3-dimethylbenzamide
Liu, Jian-hua; et al, Nongyao, 2013, 52(11), 793-795

2-Amino-N,3-dimethylbenzamide Raw materials

2-Amino-N,3-dimethylbenzamide Preparation Products

2-Amino-N,3-dimethylbenzamide Suppliers

Suzhou Senfeida Chemical Co., Ltd
Gold Member
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(CAS:870997-57-2)Methyl 2-amino-3-methylbenzoate
Order Number:1633662
Stock Status:in Stock
Quantity:Company Customization
Purity:98%
Pricing Information Last Updated:Monday, 14 April 2025 21:49
Price ($):discuss personally
Amadis Chemical Company Limited
Gold Member
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(CAS:870997-57-2)2-Amino-N,3-dimethylbenzamide
Order Number:A841952
Stock Status:in Stock
Quantity:1kg/500g
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 06:54
Price ($):379.0/223.0
Tiancheng Chemical (Jiangsu) Co., Ltd
Gold Member
Audited Supplier Audited Supplier
(CAS:870997-57-2)2-氨基-N，3-二甲基苯甲酰胺
Order Number:LE1633662
Stock Status:in Stock
Quantity:25KG,200KG,1000KG
Purity:99%
Pricing Information Last Updated:Friday, 20 June 2025 12:29
Price ($):discuss personally

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Suzhou Senfeida Chemical Co., Ltd
(CAS:870997-57-2)Methyl 2-amino-3-methylbenzoate
1633662
Purity:98%
Quantity:Company Customization
Price ($):Inquiry
Email
Amadis Chemical Company Limited
(CAS:870997-57-2)2-Amino-N,3-dimethylbenzamide
A841952
Purity:99%/99%
Quantity:1kg/500g
Price ($):379.0/223.0
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