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36719-69-4

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36719-69-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36719-69-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,7,1 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 36719-69:
(7*3)+(6*6)+(5*7)+(4*1)+(3*9)+(2*6)+(1*9)=144
144 % 10 = 4
So 36719-69-4 is a valid CAS Registry Number.

36719-69-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-Methoxyphenyl)-3,3-diethyl-1-triazene

1.2 Other means of identification

Product number -
Other names 1-(4-methoxyphenyl)-3,3-diethyltriazene

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:36719-69-4 SDS

36719-69-4Relevant articles and documents

Palladium-catalyzed direct C2 arylation of N-substituted indoles with 1-aryltriazenes

Liu, Can,Miao, Tao,Zhang, Lei,Li, Pinhua,Zhang, Yicheng,Wang, Lei

, p. 2584 - 2589 (2014)

A novel and efficient palladium-catalyzed C2 arylation of N-substituted indoles with 1-aryltriazenes for the synthesis of 2-arylindoles was developed. In the presence of BF3?OEt2 and palladium(II) acetate (Pd(OAc)2), N-substituted indoles reacted with 1-aryltriazenes in N,N-dimethylacetamide (DMAC) to afford the corresponding aryl-indole-type products in good to excellent yields.

Sulfide synthesis through copper-catalyzed C-S bond formation under biomolecule-compatible conditions

Zhang, Yonghong,Li, Yiming,Zhang, Xiaomei,Jiang, Xuefeng

supporting information, p. 941 - 944 (2015/01/09)

We report here an efficient and mild method for constructing C-S bonds. The reactions were carried out with Na2S2O3 as a sulfurating reagent, CuSO4 as a catalyst, and water as solvent without any surfactant. The products were achieved in moderate to excellent yields at room temperature under air. Notably, this reaction is compatible with various biomolecules including amino acids, oligosaccharides, nucleosides, proteins, and cell lysates. This journal is

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