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16183-39-4

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16183-39-4 Usage

General Description

CHEMBRDG-BB 4024926 is a chemical compound with the molecular formula C21H20N2O2. It is a potential histone deacetylase (HDAC) inhibitor, which means it may have the ability to regulate gene expression and potentially be used in cancer therapy. This chemical has not been extensively studied, but its structure suggests that it may have biological activity, making it a potential lead compound for future drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 16183-39-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,8 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 16183-39:
(7*1)+(6*6)+(5*1)+(4*8)+(3*3)+(2*3)+(1*9)=104
104 % 10 = 4
So 16183-39-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H16ClN/c1-2-3-8-13-9-10-6-4-5-7-11(10)12/h4-7,13H,2-3,8-9H2,1H3

16183-39-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(2-chlorophenyl)methyl]butan-1-amine

1.2 Other means of identification

Product number -
Other names butyl[(2-chlorophenyl)methyl]amine

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:16183-39-4 SDS

16183-39-4Downstream Products

16183-39-4Relevant articles and documents

Reductive Amination Revisited: Reduction of Aldimines with Trichlorosilane Catalyzed by Dimethylformamide─Functional Group Tolerance, Scope, and Limitations

Campbell, Joanna L. P.,Davies, Christopher D.,Ho?ek, Jan,Ko?ovsky, Pavel,Kysilka, Ond?ej,Popov, Kirill K.,Pour, Milan

, p. 920 - 943 (2022/01/27)

Aldimines, generated in situ from aliphatic, aromatic, and heteroaromatic aldehydes and aliphatic, aromatic, and heteroaromatic primary or secondary amines, can be reduced with trichlorosilane in the presence of dimethylformamide (DMF) as an organocatalys

Antiatherosclerotic ureas and thioureas

-

, (2008/06/13)

This invention is concerned with ureas and thioureas which may be represented by the formula: STR1 wherein X represents at least one substituent selected from the group consisting of (C1 -C4)alkyl, (C1 -C4)alken

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