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Benzeneacetic acid, a-3-butynyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88071-01-6

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88071-01-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88071-01-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,0,7 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 88071-01:
(7*8)+(6*8)+(5*0)+(4*7)+(3*1)+(2*0)+(1*1)=136
136 % 10 = 6
So 88071-01-6 is a valid CAS Registry Number.

88071-01-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-5-hexynoic acid

1.2 Other means of identification

Product number -
Other names 2-phenylhex-5-ynoic acid

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:88071-01-6 SDS

88071-01-6Relevant academic research and scientific papers

Haloenol pyranones and morpholinones as antineoplastic agents of prostate cancer

Mock, Jason N.,Taliaferro, John P.,Lu, Xiao,Patel, Sravan Kumar,Cummings, Brian S.,Long, Timothy E.

scheme or table, p. 4854 - 4858 (2012/08/13)

Haloenol pyran-2-ones and morpholin-2-ones were synthesized and evaluated as inhibitors of cell growth in two different prostate human cancer cell lines (PC-3 and LNCaP). Analogs derived from l- and d-phenylglycine were found to be the most effective antagonists of LNCaP and PC-3 cell growth. Additional studies reveal that the inhibitors induced G2/M arrest and the (S)-enantiomer of the phenylglycine-based derivatives was a more potent inhibitor of cytosolic iPLA2β.

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