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147687-45-4

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147687-45-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147687-45-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,6,8 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 147687-45:
(8*1)+(7*4)+(6*7)+(5*6)+(4*8)+(3*7)+(2*4)+(1*5)=174
174 % 10 = 4
So 147687-45-4 is a valid CAS Registry Number.

147687-45-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(hydroxy(phenyl)methyl)acrylic acid

1.2 Other means of identification

Product number -
Other names -

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:147687-45-4 SDS

147687-45-4Relevant articles and documents

Factors influencing the cytotoxicity of α-methylene-γ-hydroxy esters against pancreatic cancer

Ramachandran, P. Veeraraghavan,Helppi, Matthew A.,Lehmkuhler, Arlie L.,Marchi, Jennifer M.,Schmidt, C. Max,Yip-Schneider, Michele T.

, p. 4270 - 4273 (2015/11/03)

A systematic study to identify the factors influencing the cytotoxicity of α-methylene-γ-hydroxy esters against three pancreatic cancer cell lines (Panc-1, MIA-PaCa-2, and BxPC-3) has established that, in addition to Michael acceptor abilities, the possibility to lactonize to α-methylene-γ-butyrolactones is as important. The substitution pattern and the number of carbons between the hydroxy and ester moieties also influence the bio-activity.

Decarboxylative heck reaction of aryl iodide with baylis-hillman adduct using PD/C as a catalyst in aqueous media

Kim, Hyun-Soo,Lee, Sang-Jin,Yoon, Cheol Min

, p. 325 - 327 (2013/08/24)

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A novel liquid-phase synthesis of Baylis-Hillman products using PEG-supported α-phenylselenopropionate ester

Sheng, Shou-Ri,Wang, Qiong,Wang, Qiu-Ying,Guo, Lei,Liu, Xiao-Ling,Huang, Xian

, p. 1887 - 1890 (2008/02/08)

Treatment of the lithio derivative of novel PEG-supported α-phenylselenopropionate ester with aldehydes and subsequent cleavage from the PEG support by oxidative elimination with 30% hydrogen peroxide efficiently afforded Baylis-Hillman products in good y

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