2-AMINO-1-METHYLBENZIMIDAZOLE

2-AMINO-1-METHYLBENZIMIDAZOLE Structure
CAS No.
1622-57-7
Chemical Name:
2-AMINO-1-METHYLBENZIMIDAZOLE
Synonyms
AKOS B000495;ART-CHEM-BB B000495;TIMTEC-BB SBB004092;RARECHEM AQ NN 0081;1-methyl-2-benzimidazolamine;1-methylbenzimidazol-2-amine;2-AMINO-1-METHYLBENZIMIDAZOLE;1-methyl-2-aminobenzimidazole;1-methyl-1h-benzimidazol-2-amin;1-methyl-1h-benzimidazol-2-amine
CBNumber:
CB9743322
Molecular Formula:
C8H9N3
Molecular Weight:
147.18
MOL File:
1622-57-7.mol
MSDS File:
SDS
Modify Date:
2023/5/25 10:25:49

2-AMINO-1-METHYLBENZIMIDAZOLE Properties

Melting point 203-206 °C
Boiling point 257.29°C (rough estimate)
Density 1.1669 (rough estimate)
refractive index 1.5400 (estimate)
storage temp. 2-8°C(protect from light)
form Fine Crystalline Powder
pka 6.96±0.10(Predicted)
color White to beige
CAS DataBase Reference 1622-57-7(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-37/39
WGK Germany  3
RTECS  DD5423660
HazardClass  IRRITANT
HS Code  29339980
NFPA 704
0
1 0

2-AMINO-1-METHYLBENZIMIDAZOLE price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 412546 2-Amino-1-methylbenzimidazole 95% 1622-57-7 1G ₹7390 2022-06-14 Buy
Sigma-Aldrich(India) 412546 2-Amino-1-methylbenzimidazole 95% 1622-57-7 5G ₹19560 2022-06-14 Buy
Product number Packaging Price Buy
412546 1G ₹7390 Buy
412546 5G ₹19560 Buy

2-AMINO-1-METHYLBENZIMIDAZOLE Chemical Properties,Uses,Production

Chemical Properties

white to beige fine crystalline powder

Uses

2-Amino-1-methylbenzimidazole may be used for the preparation of 2- or 3-carboxy-4H-pyrimido[2,1-b]-benzazol-4-ones and novel functionalized spiropyran′s derivatives of 2H-1,3-benzoxazinone series.

General Description

The carbonyl-scavenging ability of 2-amino-1-methylbenzimidazole has been investigated. Mechanism of Menshutkin reaction between 2-amino-1-methylbenzimidazole and iodomethane has been studied in gas phase and in liquid acetonitrile. It is reported to form adducts with natural allyl, phenethyl, and benzyl isothiocyanates.

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1-methyl-1h-benzimidazol-2-amin 1-methyl-1h-benzimidazol-2-amine 1-methyl-2-aminobenzimidazole ART-CHEM-BB B000495 AKOS B000495 1-METHYL-1 H-BENZOIMIDAZOL-2-YLAMINE 1-METHYL-1H-BENZO[D]IMIDAZOL-2-AMINE 2-AMINO-1-METHYLBENZIMIDAZOLE RARECHEM AQ NN 0081 TIMTEC-BB SBB004092 1H-Benzimidazol-2-amine,1-methyl-(9CI) 2-AMINO-1-METHYLBENZO(1,2-D)IMIDAZOLE 2-AMINO-1-METHYLBENZIMIDAZOLE 99+% 1H-benzimidazol-2-amine, 1-methyl- 1-methyl-1H-benzimidazol-2-amine(SALTDATA: FREE) 2-AMino-1-MethylbenziMidazole 95% (1-methylbenzimidazol-2-yl)amine 1-methyl-2-benzimidazolamine 1-methylbenzimidazol-2-amine Benzimidazole, 2-amino-1-methyl- 2-AMino-1-MethylbenziMidazole, 99+% 2.5GR 2-Amino-1-methyl-1H-benzimidazole 1-METHYL-1H-BENZO[D]IMIDAZOL-2-A 1622-57-7 Building Blocks Benzimidazoles Heterocyclic Building Blocks AMINE BENZIMIDAZOLE pharmacetical Benzimidazoles Building Blocks Heterocyclic Building Blocks