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101506-39-2

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101506-39-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101506-39-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,5,0 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 101506-39:
(8*1)+(7*0)+(6*1)+(5*5)+(4*0)+(3*6)+(2*3)+(1*9)=72
72 % 10 = 2
So 101506-39-2 is a valid CAS Registry Number.

101506-39-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-octylcarbamate

1.2 Other means of identification

Product number -
Other names tert-butyl octylcarbamate

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:101506-39-2 SDS

101506-39-2Relevant articles and documents

Synthesis of carbamates from amines and dialkyl carbonates: Influence of leaving and entering groups

Tundo, Pietro,McElroy, C. Robert,Aricò, Fabio

, p. 1567 - 1571 (2010)

A number of carbamates were synthesised through a halogen-free process by reacting amines with symmetrical and unsymmetrical carbonates. The results obtained showed a specific trend of preferred leaving groups (in the dialkyl carbonates) depending on whether a catalyst or a base was used. On the other hand, investigations conducted on the preferred entering groups (amines) for the synthesis of carbamates showed the same trend regardless of whether a catalyst or a base was used. Finally, in accordance with the results obtained, it was possible to synthesise sterically hindered carbamates in high yield by transesterification of methyl carbamate with a sterically hindered alcohol. Georg Thieme Verlag Stuttgart New York.

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