Welcome to LookChem.com Sign In|Join Free

CAS

  • or
2-Benzyl-1H-benzimidazole monohydrochloride is a hydrochloride salt of 2-benzyl-1H-benzimidazole, a benzimidazole derivative with potential anti-tumor and anti-cancer properties. It is a chemical compound often used in pharmaceutical research and development, known for its potential effects on inhibiting the growth of cancer cells and suppressing tumor growth.
Used in Pharmaceutical Research and Development:
2-Benzyl-1H-benzimidazole monohydrochloride is used as a potential anti-cancer agent for its potential effects on inhibiting the growth of cancer cells and suppressing tumor growth.
Used in Oncology:
2-Benzyl-1H-benzimidazole monohydrochloride is used as a potential treatment for gastrointestinal cancer and other types of solid tumors due to its anti-tumor properties.
Used in Pharmaceutical Formulation:
The hydrochloride salt form of 2-benzyl-1H-benzimidazole makes it more stable and soluble, which is beneficial for formulation in pharmaceutical applications, enhancing its potential use in drug development.

1212-48-2

Post Buying Request

1212-48-2 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1212-48-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1212-48-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,1 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1212-48:
(6*1)+(5*2)+(4*1)+(3*2)+(2*4)+(1*8)=42
42 % 10 = 2
So 1212-48-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H12N2.ClH/c1-2-6-11(7-3-1)10-14-15-12-8-4-5-9-13(12)16-14;/h1-9H,10H2,(H,15,16);1H

1212-48-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzyl-1H-benzimidazole,hydrochloride

1.2 Other means of identification

Product number -
Other names 2-benzyl-1H-benzimidazole hydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1212-48-2 SDS

1212-48-2Downstream Products

1212-48-2Relevant articles and documents

Synthesis method of dibazolum

-

Paragraph 0024; 0025; 0026; 0027, (2017/01/17)

The invention provides a synthesis method of dibazolum. The synthesis method comprises the following steps: adding o-phenylenediamine and toluene into a reaction container; dropwise adding phenylacetyl chloride into the reaction container; after dripping, heating and reflowing to react until the reaction is finished; carrying out post-treatment to obtain a dibazolum product. Compared with the prior art, the synthesis method has the following beneficial technical effects that (1) the reaction temperature is reduced so that a reaction for synthesizing the dibazolum can be carried out under a moderate condition; (2) any hydration agent or any catalyst is not added in the synthesis method and side reactions are few, so that impurities are effectively reduced and the number of times of subsequent de-coloring and crystallization is reduced; (3) post-treatment operation is simplified by the synthesis method so that the production cost is saved and large-scale and industrial production is facilitated.

Synthesis of nitrogenous heterocycles under microwave activation

El'tsov,Sokolova,Dmitrieva,Grigor'ev,Ivanov

, p. 1317 - 1320 (2007/10/03)

Microvawe activation accelerates heterocyclization of o-phenylenediamine with phenylacetic acid with benzyl cyanide tens times, simultaneously improving the yield and quality of the resulting 2-benzyl-imidazole. The effect of microwave activation on heterocyclization of ethyl(phenyl)malonic acid with formic acid or its amide is not so strong.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 1212-48-2