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179314-60-4

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179314-60-4 Usage

Chemical compound

2-Amino-6-bromo-4-chlorophenol

Check Digit Verification of cas no

The CAS Registry Mumber 179314-60-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,3,1 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 179314-60:
(8*1)+(7*7)+(6*9)+(5*3)+(4*1)+(3*4)+(2*6)+(1*0)=154
154 % 10 = 4
So 179314-60-4 is a valid CAS Registry Number.

179314-60-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-6-bromo-4-chlorophenol

1.2 Other means of identification

Product number -
Other names 6-amino-2-bromo-4-chloro-phenol

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:179314-60-4 SDS

179314-60-4Downstream Products

179314-60-4Relevant articles and documents

COMPOUNDS AND COMPOSITIONS AS RAF KINASE INHIBITORS

-

, (2016/04/20)

The present invention provides compounds of Formula (I) and (II) as described herein, and salts thereof, and therapeutic uses of these compounds for treatment of disorders associated with Raf kinase activity. The invention further provides pharmaceutical compositions comprising these compounds, and compositions comprising these compounds and a therapeutic co-agent.

6,5-Fused aromatic ring systems having enhanced phosphodiesterae IV inhibitory activity

-

, (2008/06/13)

Novel compounds which are effective PDE IV inhibitors are disclosed. The compounds possess improved PDE IV inhibition as compared to theophylline or rolipram, with improved selectivity with regard to, e.g., PDE V inhibition. The present invention includes compounds of Formula I: wherein:rings "A" and "B" can be saturated, unsaturated or partially unsaturated;X1 is selected from CH, C-Cl, or N;X2 is selected from CR12 or N;X3 is selected from CH or N;X4 is selected from CH or N;P1, P2 are independently selected from CH,O or N or NH;M is selected from CH, C, or N;Q is C1-C3 alkyl or -CH=CH-;R6 is selected from -C(R9)3, CH(R9)2, or C3-C8 cycloalkyl;R7 is selected from -OH, -O-CO-CH3, -SH, or -CHO;R8 is selected from -C(R9)3, -CH(R9)2, -C3-C8-cycloalkyl, or -CH2-C4-C6-cycloalkyl;R10 is selected from C1-C3-pyridyl, C3H6OH,-C= C-, Br, -C=C-CH2OH, isopropyl, hydrogen, andR11 is selected from H, -OH, -O-C3-C8-cycloalkyl, -NH2, -NH-C1-C3-alkyl, -SH, -NH-C3-C8-cycloalkyl, -Z-pyridyl, -Z-trienyl, and -Z-CH2OH;R12 is selected from -SH, H, halogen or lower alkyl;R9 is lower alkyl; andZ is selected from ethyl, and -C=C-.

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