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Bicyclo[2.2.1]heptan-2-ol, 3,3'-dithiobis[1,7,7-trimethyl-, (1R,1'R,2S,2'S,3R,3'R,4S,4'S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

502917-77-3

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502917-77-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 502917-77-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,2,9,1 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 502917-77:
(8*5)+(7*0)+(6*2)+(5*9)+(4*1)+(3*7)+(2*7)+(1*7)=143
143 % 10 = 3
So 502917-77-3 is a valid CAS Registry Number.

502917-77-3SDS

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 (1R,2S,3R)-bis(2-hydroxybornane-3-yl)disulfide

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:502917-77-3 SDS

502917-77-3Relevant academic research and scientific papers

Application of New Camphor-Derived Mercapto Chiral Auxiliaries to the Synthesis of Optically Active Primary Amines

Yang, Teng-Kuei,Chen, Ruey-Yuan,Lee, Dong-Sheng,Peng, Wen-Shiuan,Jiang, Yao-Zhong,et al.

, p. 914 - 921 (2007/10/02)

A series enantiomerically pure sulfinimines carrying new camphor-based mercapto chiral auxiliaries are subjected to assymetric alkylation.Such reaction offers an excellent route to the preparation of optically active primary amines.Also reported here is an unprecedented Grignard addition of a chiral sulfenimine leading to a single enantiomer of the corresponding sulfenamide and thence produced enantiopure amine after acidic aqueous workup.The chiral auxiliary can be recovered in high yield.

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