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CHEMBRDG-BB 4010741 is a benzodiazole derivative with the molecular formula C13H10N2O3, also known as 1-((1-benzyl-1H-1,2,3-triazol-4-yl)methyl)-2-(2,4-dinitrophenyl)methyl-1H-1,3-benzodiazole. It belongs to the benzodiazole family, which has been studied for their therapeutic potential in various diseases. CHEMBRDG-BB 4010741 has been the subject of research and development efforts for its potential use in cancer treatment due to its ability to inhibit the growth of cancer cells.

92322-05-9

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92322-05-9 Usage

Uses

Used in Pharmaceutical Industry:
CHEMBRDG-BB 4010741 is used as a potential anti-cancer and anti-tumor agent for its ability to inhibit the growth of cancer cells. It is currently under research and development to fully understand its potential applications and mechanisms of action in cancer treatment.

Check Digit Verification of cas no

The CAS Registry Mumber 92322-05-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,3,2 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 92322-05:
(7*9)+(6*2)+(5*3)+(4*2)+(3*2)+(2*0)+(1*5)=109
109 % 10 = 9
So 92322-05-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H21NO/c16-12-14-7-4-9-15(11-14)10-8-13-5-2-1-3-6-13/h1-3,5-6,14,16H,4,7-12H2

92322-05-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name [1-(2-phenylethyl)piperidin-3-yl]methanol

1.2 Other means of identification

Product number -
Other names N-Phenethyl-3-hydroxymethylpiperidin

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:92322-05-9 SDS

92322-05-9Downstream Products

92322-05-9Relevant academic research and scientific papers

An efficient method for reductive amination of carbonyl compounds under nonacidic conditions

Hudson, Julian A.,Sweeney

, p. 2176 - 2178 (2012/10/29)

A high yielding reductive amination procedure for ketones and aldehydes under neutral conditions is described. The key advantage for the method is the applicability to acid-sensitive substrates, and the procedure is applicable to a wide range of primary and secondary amines, on a multigram scale. Georg Thieme Verlag Stuttgart ? New York.

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