- Preparation of benzoimidazolylmethylpyrimidinediamine derivatives and analogs for use as serine/threonine PAK1 inhibitors, World Intellectual Property Organization, , ,
Cas no 952511-48-7 (5-bromo-4-methyl-1H-benzodimidazole)
952511-48-7 structure
Product Name:5-bromo-4-methyl-1H-benzodimidazole
CAS No:952511-48-7
MF:C8H7BrN2
MW:211.058580636978
MDL:MFCD18642426
CID:1035817
PubChem ID:59214444
Update Time:2024-10-25
5-bromo-4-methyl-1H-benzodimidazole Chemical and Physical Properties
Names and Identifiers
-
- 5-Bromo-4-methyl-1H-benzo[d]imidazole
- 5-bromo-4-methyl-1H-benzimidazole
- AK118838
- 5-Bromo-4-methylbenzimidazole
- JNXOUOKRAGYUNE-UHFFFAOYSA-N
- 6-bromo-7-methyl-1H-benzimidazole
- 6383AC
- FCH1335720
- OR19568
- AB0070067
- ST2406138
- AX8244254
- 6-Bromo-7-methyl-1H-benzimidazole (ACI)
- MFCD18642426
- DB-368544
- CS-W022329
- 952511-48-7
- AKOS016000450
- DS-5412
- C77285
- SCHEMBL1798450
- DTXSID50731276
- CNB51148
- 5-bromo-4-methyl-1H-benzodimidazole
-
- MDL： MFCD18642426
- Inchi： 1S/C8H7BrN2/c1-5-6(9)2-3-7-8(5)11-4-10-7/h2-4H,1H3,(H,10,11)
- InChI Key： JNXOUOKRAGYUNE-UHFFFAOYSA-N
- SMILES： BrC1C(C)=C2C(N=CN2)=CC=1
Computed Properties
- Exact Mass: 209.97900
- Monoisotopic Mass: 209.97926g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 11
- Rotatable Bond Count: 0
- Complexity: 151
- 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
- Topological Polar Surface Area: 28.7
- XLogP3: 2.5
Experimental Properties
- Density: 1.7±0.1 g/cm3
- Boiling Point: 418.3±25.0 °C at 760 mmHg
- Flash Point: 206.8±23.2 °C
- PSA: 28.68000
- LogP: 2.63380
- Vapor Pressure: 0.0±0.9 mmHg at 25°C
5-bromo-4-methyl-1H-benzodimidazole Security Information
- Signal Word：Warning
- Hazard Statement： H302-H315-H319-H332-H335
- Warning Statement： P261-P280-P305+P351+P338
- Safety Instruction： H303+H313+H333
- Storage Condition：Sealed in dry,Room Temperature
5-bromo-4-methyl-1H-benzodimidazole Customs Data
- HS CODE：2933990090
- Customs Data：
China Customs Code:
2933990090Overview:
2933990090. Other heterocyclic compounds containing only nitrogen heteroatoms. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%
Declaration elements:
Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date
Summary:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
5-bromo-4-methyl-1H-benzodimidazole Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Fluorochem | 215394-250mg |
5-Bromo-4-methyl-1H-benzo[d]imidazole |
952511-48-7 | 95% | 250mg |
￡59.00 | 2022-02-28 | |
| Fluorochem | 215394-1g |
5-Bromo-4-methyl-1H-benzo[d]imidazole |
952511-48-7 | 95% | 1g |
￡163.00 | 2022-02-28 | |
| Fluorochem | 215394-5g |
5-Bromo-4-methyl-1H-benzo[d]imidazole |
952511-48-7 | 95% | 5g |
￡661.00 | 2022-02-28 | |
| TRC | B814643-10mg |
5-bromo-4-methyl-1H-benzo[d]imidazole |
952511-48-7 | 10mg |
$ 50.00 | 2022-06-06 | ||
| TRC | B814643-50mg |
5-bromo-4-methyl-1H-benzo[d]imidazole |
952511-48-7 | 50mg |
$ 115.00 | 2022-06-06 | ||
| TRC | B814643-100mg |
5-bromo-4-methyl-1H-benzo[d]imidazole |
952511-48-7 | 100mg |
$ 160.00 | 2022-06-06 | ||
| Chemenu | CM130073-1g |
5-bromo-4-methyl-1H-benzo[d]imidazole |
952511-48-7 | 97% | 1g |
$239 | 2021-06-09 | |
| Chemenu | CM130073-5g |
5-bromo-4-methyl-1H-benzo[d]imidazole |
952511-48-7 | 97% | 5g |
$954 | 2021-06-09 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-MV617-100mg |
5-bromo-4-methyl-1H-benzodimidazole |
952511-48-7 | 97% | 100mg |
305CNY | 2021-05-08 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-MV617-250mg |
5-bromo-4-methyl-1H-benzodimidazole |
952511-48-7 | 97% | 250mg |
716CNY | 2021-05-08 |
5-bromo-4-methyl-1H-benzodimidazole Production Method
Production Method 1
Reaction Conditions
1.1 Reagents: Hydrochloric acid Solvents: Water ; 12 h, rt → 60 °C; cooled
1.2 Reagents: Ammonium hydroxide Solvents: Water ; pH 8 - 9
1.2 Reagents: Ammonium hydroxide Solvents: Water ; pH 8 - 9
Reference
Production Method 2
Reaction Conditions
1.1 3 h, reflux
Reference
- Preparation of oxadiazole compounds as S1P1 agonists, United States, , ,
Production Method 3
Reaction Conditions
1.1 Reagents: Hydrochloric acid Solvents: Water ; 18 h, reflux
Reference
- Thermodynamic parameters for binding of some halogenated inhibitors of human protein kinase CK2Winiewska, Maria; Makowska, Malgorzata; Maj, Piotr; Wielechowska, Monika; Bretner, Maria; et al, Biochemical and Biophysical Research Communications, 2015, 456(1), 282-287
Production Method 4
Reaction Conditions
1.1 Reagents: Acetic acid ; 12 h, 0 °C
1.2 Reagents: Sodium bicarbonate Solvents: Water ; pH 8
1.2 Reagents: Sodium bicarbonate Solvents: Water ; pH 8
Reference
- Azacyclodione compound and preparation and application in inhibiting cap-dependent endonuclease activity thereof, China, , ,
Production Method 5
Reaction Conditions
1.1 Reagents: Stannous chloride Solvents: Ethanol ; 2 h, 50 °C; 50 °C → rt
1.2 30 min, 70 °C; 70 °C → rt
1.2 30 min, 70 °C; 70 °C → rt
Reference
- Preparation of bicyclic heteroaryl-substituted imidazoles as modulators of the histamine H4 receptor, United States, , ,
5-bromo-4-methyl-1H-benzodimidazole Raw materials
- 1,2-Benzenediamine, 4-bromo-3-methyl-, hydrochloride (1:2)
- 1-Bromo-2-methyl-3,4-dinitrobenzene
- 4-bromo-3-methyl-benzene-1,2-diamine
5-bromo-4-methyl-1H-benzodimidazole Preparation Products
5-bromo-4-methyl-1H-benzodimidazole Related Literature
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Thi Thu Tram Nguyen,Thanh Binh Nguyen Org. Biomol. Chem., 2021,19, 6015-6020
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Nan Fu,Naphaporn Chiewchan,Xiao Dong Chen Food Funct., 2020,11, 211-220
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Ziyang Deng,Changwei Chen,Sunliang Cui RSC Adv., 2016,6, 93753-93755
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Chung-Sung Yang,Mong-Shian Shih,Fang-Yi Chang New J. Chem., 2006,30, 729-735
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5. Fatty acid eutectic mixtures and derivatives from non-edible animal fat as phase change materials?Pau Gallart-Sirvent,Marc Martín,Gemma Villorbina,Mercè Balcells,Aran Solé,Luisa F. Cabeza,Ramon Canela-Garayoa RSC Adv., 2017,7, 24133-24139
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