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(1RS,2RS,3SR,4SR)-1,2,3,4-tetrakis(((tolyl-4-sylfonyl)oxy)methyl)cyclopentane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62349-01-3

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62349-01-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62349-01-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,3,4 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62349-01:
(7*6)+(6*2)+(5*3)+(4*4)+(3*9)+(2*0)+(1*1)=113
113 % 10 = 3
So 62349-01-3 is a valid CAS Registry Number.

62349-01-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (1RS,2RS,3SR,4SR)-1,2,3,4-tetrakis(((tolyl-4-sylfonyl)oxy)methyl)cyclopentane

1.2 Other means of identification

Product number -
Other names all-cis-1,2,3,4-tetra(tosyloxymethyl)cyclopentane

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:62349-01-3 SDS

62349-01-3Relevant articles and documents

A new tetratertiary phosphine ligand and its use in Pd-catalyzed allylic substitution

Laurenti,Feuerstein,Pepe,Doucet,Santelli

, p. 1633 - 1637 (2007/10/03)

A new tetraphosphine, the cis-cis-cis-1,2,3,4-tetrakis(diphenylphosphinomethyl)cyclopentane (Tedicyp) 1 has been synthesized, characterized, and used in Pd-catalyzed allylic substitutions. The Tedicyp was easily prepared in seven steps from the commercially available himic anhydride. The structure of the complex Tedicyp-borane was determined by X-ray analysis. The tetraphosphine in combination with [Pd(η3-C3H5)Cl]2 affords a very efficient catalyst for allylic substitution of several allylic acetates. Under mild conditions, very high turnover numbers and turnover frequencies have been obtained.

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