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Valine, N-[[4-[bis(2-chloroethyl)amino]phenyl]acetyl]-, also known as Chlorambucil, is an organic compound with the chemical formula C14H19Cl2NO2. It is a derivative of the amino acid valine and is primarily used as an anticancer drug. Chlorambucil works by inhibiting DNA synthesis and function, leading to the death of cancer cells. It is particularly effective in treating chronic lymphocytic leukemia, Hodgkin's lymphoma, and other lymphomas. The compound is a white crystalline solid and is soluble in various organic solvents. Due to its potential side effects, including bone marrow suppression and gastrointestinal issues, it is administered under the supervision of a healthcare professional.

10053-76-6

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10053-76-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10053-76-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,5 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10053-76:
(7*1)+(6*0)+(5*0)+(4*5)+(3*3)+(2*7)+(1*6)=56
56 % 10 = 6
So 10053-76-6 is a valid CAS Registry Number.

10053-76-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4--phenylacetyl)-D,L-valin

1.2 Other means of identification

Product number -
Other names N-{4-[Bis-(2-chlor-aethyl)-amino]-phenylacetyl}-D,L-valin

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:10053-76-6 SDS

10053-76-6Upstream product

10053-76-6Downstream Products

10053-76-6Relevant academic research and scientific papers

Synthesis of optical antipodes of N-p-[di-(2-chloroethyl)amino]phenacetylamino acids

Klyukene,Karpavichyus,Kil'disheva

, p. 870 - 872 (2007/10/05)

The optical antipodes of N-p-[di-(2-chloroethyl)amino]phenacetylvaline, methionine, and alanine were obtained by the acid chloride and N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline methods; the carbodiimide method and the activated cyanomethyl ester meth

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