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Benzoic acid, 4-methoxy-, 3-hexenyl ester, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

121432-33-5

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121432-33-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121432-33-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,4,3 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 121432-33:
(8*1)+(7*2)+(6*1)+(5*4)+(4*3)+(3*2)+(2*3)+(1*3)=75
75 % 10 = 5
So 121432-33-5 is a valid CAS Registry Number.

121432-33-5SDS

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-methyl-N-(nitrosomethyl)butan-1-amine

1.2 Other means of identification

Product number -
Other names N-Nitrosomethyl(2-methylbutyl)amine

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:121432-33-5 SDS

121432-33-5Downstream Products

121432-33-5Relevant academic research and scientific papers

Catalytic Regio- and Enantioselective Oxytrifluoromethylthiolation of Aliphatic Internal Alkenes by Neighboring Group Assistance

Xu, Jia,Zhang, Yuanyuan,Qin, Tian,Zhao, Xiaodan

, p. 6384 - 6388 (2018/10/09)

Chiral selenide-catalyzed oxytrifluoromethylthiolation of aliphatic internal alkenes by a formally intermolecular strategy is disclosed, affording CF3S 1,3-amino alcohol and 1,3-diol derivatives with high regio-, enantio-, and diastereoselectivities. The reactions are promoted by a neighboring imide or ester group on substrates via a six-membered ring transition state. This assistance strategy is also successfully applied to the regio- and diastereoselective oxyhalofunctionalization of internal alkenes and the conversion of alkynes.

Cobalt-Catalyzed Esterification of Amides

Bourne-Branchu, Yann,Gosmini, Corinne,Danoun, Grégory

supporting information, p. 10043 - 10047 (2017/08/01)

The first cobalt-catalyzed amide activation of N-Boc-amides, and their conversion into esters, is reported here. This new methodology presents a very practical process that does not require an inert atmosphere, uses an inexpensive cobalt catalyst, and proceeds under mild reaction conditions. This catalytic system has a broad substrate scope and has been shown to be highly efficient, with catalyst loadings as low as 1 mol %.

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