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Carbamic acid, dimethyl-, 2,4,6-tris(1,1-dimethylethyl)phenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65832-33-9

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65832-33-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65832-33-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,8,3 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 65832-33:
(7*6)+(6*5)+(5*8)+(4*3)+(3*2)+(2*3)+(1*3)=139
139 % 10 = 9
So 65832-33-9 is a valid CAS Registry Number.

65832-33-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,4,6-tritert-butylphenyl) N,N-dimethylcarbamate

1.2 Other means of identification

Product number -
Other names Carbamic acid,dimethyl-,2,4,6-tris(1,1-dimethylethyl)phenyl ester

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:65832-33-9 SDS

65832-33-9Relevant academic research and scientific papers

Copper porphyrin-catalyzed C(sp2)—O bond construction via coupling phenols with formamides

Yang, Shuang,Chen, Xiao-Yan,Xiong, Ming-Feng,Zhang, Hao,Shi, Lei,Lin, Dong-Zi,Liu, Hai-Yang

, p. 1541 - 1548 (2021/04/21)

Copper porphyrin-catalyzed construction of C(sp2)—O bond via coupling formamides with phenols was achieved firstly. A broad range of substrates afforded various carbamates in moderate to good yields with good functional group tolerance at low catalyst loading. Intermolecular competing kinetic isotope effect experiment indicated that the generation of formamide radical is the rate-determining step of current cross-dehydrogenative coupling (CDC) reaction. The research extends the application of metalloporphyrin in CDC reaction.

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