Details
Manufacturer supply top purity 5-(1H-Pyrrol-1-yl)-2-mercaptobenzimidazole 172152-53-3 with GMP standards
- Molecular Formula: C11H9N3S
- Molecular Weight: 215.279
- Boiling Point: 381.7±44.0 °C(Predicted)
- PKA: 9.61±0.30(Predicted)
- PSA: 72.41000
- Density: 1.40
- LogP: 2.64230
172152-53-3 Relevant articles
Diversified synthesis of novel quinoline and dibenzo thiazepine derivatives using known active intermediates
Sharada,Satyanarayana Reddy,Sammaiah,Sumalatha
, p. 7959 - 7966 (2013/09/23)
The novel drug development to control re...
PROCESS FOR PREPARING INTERMEDIATE COMPOUND FOR SYNTHESIZING AN ANTIULCERANT
-
Page/Page column 3, (2011/04/18)
The present invention relates a novel me...
PROCESS FOR PREPARING INTERMEDIATE COMPOUND FOR SYNTHESIZING AN ANTIULCERANT
-
Page 5-6, (2010/01/07)
The present invention relates a novel me...
172152-53-3 Process route
-
-
696-59-3
cis,trans-2,5-dimethoxytetrahydrofuran
-
-
2818-66-8
5-amino-2-mercaptobenzimidazole
-
-
172152-53-3
5-(1H-pyrrol-1-yl)-1H-benzo[d]imidazole-2-thiol
| Conditions | Yield |
|---|---|
|
With
sodium acetate;
In
acetic acid;
at 50 ℃;
for 4h;
Product distribution / selectivity;
|
85%
|
|
cis,trans-2,5-dimethoxytetrahydrofuran; 5-amino-2-mercaptobenzimidazole;
With
acetic acid;
at 50 ℃;
for 4h;
With
sodium hydroxide;
In
tetrahydrofuran; water;
at 5 ℃;
Product distribution / selectivity;
|
85%
|
|
With
acetic acid;
|
-
-
6325-91-3
5-nitro-2-mercaptobenzimidazole
-
-
172152-53-3
5-(1H-pyrrol-1-yl)-1H-benzo[d]imidazole-2-thiol
| Conditions | Yield |
|---|---|
|
Multi-step reaction
with
2
steps
1: hydrogenchloride; iron / water; ethanol / Reflux
2: acetic acid
With
hydrogenchloride; iron; acetic acid;
In
ethanol; water;
|
172152-53-3 Upstream products
-
696-59-3
cis,trans-2,5-dimethoxytetrahydrofuran
-
2818-66-8
5-amino-2-mercaptobenzimidazole
-
6325-91-3
5-nitro-2-mercaptobenzimidazole
172152-53-3 Downstream products
-
172152-35-1
2-(((4-methoxy-3-methylpyridin-2-yl)methyl)thio)-5-(1H-pyrrol-1-yl)-1H-benzo[d]imidazole
Related Products
-
5-Bromoacetyl-2-bensyloxybenzoic acid methyl ester
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