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66693-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66693-07-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,6,9 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 66693-07:
(7*6)+(6*6)+(5*6)+(4*9)+(3*3)+(2*0)+(1*7)=160
160 % 10 = 0
So 66693-07-0 is a valid CAS Registry Number.

66693-07-0SDS

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 2-benzenesulfonyl-3-phenyl-propionic acid ethyl ester

1.2 Other means of identification

Product number -
Other names inakt. α-Phenylsulfon-hydrozimtsaeure-aethylester

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:66693-07-0 SDS

66693-07-0Relevant articles and documents

FLP-catalysis meets hydrogen-bond activation

K?ring, Laura,Paradies, Jan,Roesky, Peter W.,Sitte, Nikolai A.

supporting information, p. 7321 - 7325 (2020/10/13)

The potential of two chiral amidines and three non-chiral boranes in the metal-free hydrogen activation was explored. The resulting chiral amidiunium borohydride salts were investigated in asymmetric hydrogenation reactions of ketimines, activated double bonds and dehydro amioacid esters.

Solid-liquid phase transfer catalytic synthesis V III: The rapid alkylation of ethyl phenylsulfonylacetate under microwave irradiation

Wang,Jiang

, p. 2287 - 2291 (2007/10/02)

Rapid alkylations of ethyl phenylsufonylacetate with a series of halides were performed in 960 W domestic microwave oven, and the isolated yield of α-monoalkylated product varying from 76 to 86%.

Chemistry of Novel Compounds with Multifunctional Carbon Structure. 5. Molecular Design of Versatile Building Blocks for Aliphatic Monofluoro Molecules by Manipulation of Multifunctional Carbon Structure

Takeuchi, Yoshio,Nagata, Kazuhiro,Koizumi, Toru

, p. 5453 - 5459 (2007/10/02)

Three kinds of doubly functionalized monofluoromethylene fragments, 1-fluoro-1-nitro-1-(phenylsulfonyl)alkanes (10), 2-fluoro-2-(phenylsulfonyl)alkanoic esters (11), and 2-fluoro-2-nitroalkanoic esters (12), potentially versatile building blocks for the general synthesis of various aliphatic monofluoro molecules, were prepared from the corresponding difunctional compounds 1-3 by monoalkylation (R) and selective fluorinations.The interconversion or reductive removal of each functional group in 10-12 followed by the introduction of the second alkyl groups (R') at the fluorine-bearing carbon atom was examined.Compounds 12 proved to be useful and practical building blocks for conversions to the various monofluoroalkanes 20-26.

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