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112966-96-8

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112966-96-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112966-96-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,9,6 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 112966-96:
(8*1)+(7*1)+(6*2)+(5*9)+(4*6)+(3*6)+(2*9)+(1*6)=138
138 % 10 = 8
So 112966-96-8 is a valid CAS Registry Number.
InChI:InChI=1/C20H27NO4S/c22-19(23)11-7-2-1-6-10-18-15-12-13-16(14-15)20(18)21-26(24,25)17-8-4-3-5-9-17/h1,3-6,8-9,15-16,18,20-21H,2,7,10-14H2,(H,22,23)/b6-1-/t15-,16+,18+,20+/m1/s1

112966-96-8SDS

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 (5Z)-7-{(1R,2S,3S,4S)-3-[(Phenylsulfonyl)amino]bicyclo[2.2.1]hept -2-yl}-5-heptenoic acid

1.2 Other means of identification

Product number -
Other names (+)-(5S,10S)-12-hydroxypodocarpa-8,11,13-triene

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:112966-96-8 SDS

112966-96-8Relevant articles and documents

Enantioselective synthesis of S-1452, an orally active potent thromboxane A2 receptor antagonist

Ohtani,Matsuura,Watanabe,Narisada

, p. 2122 - 2127 (2007/10/02)

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Synthesis and in vitro activity of stereoisomers of a novel thromboxane receptor antagonist, (±)-(5Z)-7-[3-endo-[(phenylsulfonyl)amino]bicyclo[2.2.1]hept-2-exo-yl ]heptenoic acid

Ohtani,Narisada

, p. 1027 - 1031 (2007/10/02)

Three stereoisomers of S-145 (1) with variations at the side-chain junctions were synthesized. Endo-cis-isomer 10 and N-exo-trans isomer 18 were obtained via the common intermediate 5 having an endo-fused ring structure. Exo-cis isomer 28 was prepared via

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