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3-methylbut-2-en-1-yl carbamate, also known as prenyl carbamate, is an organic compound with the chemical formula C6H9NO2. It is a derivative of 3-methylbut-2-en-1-ol (also known as prenol), where the hydroxyl group is replaced by a carbamate group. 3-methylbut-2-en-1-yl carbamate is of interest in organic chemistry and pharmaceutical research due to its potential applications as a chemical intermediate or a precursor in the synthesis of various biologically active compounds. Prenyl carbamate is characterized by its unique structure, which includes a carbon-carbon double bond and a methyl group, giving it specific reactivity and properties that can be exploited in chemical reactions.

36883-22-4

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36883-22-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36883-22-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,8,8 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 36883-22:
(7*3)+(6*6)+(5*8)+(4*8)+(3*3)+(2*2)+(1*2)=144
144 % 10 = 4
So 36883-22-4 is a valid CAS Registry Number.

36883-22-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methylbut-2-enyl carbamate

1.2 Other means of identification

Product number -
Other names Prenylcarbamat

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:36883-22-4 SDS

36883-22-4Downstream Products

36883-22-4Relevant academic research and scientific papers

Substrate scope and stereocontrol in the Rh(II)-catalysed oxyamination of allylic carbamates

Unsworth, William P.,Lamont, Scott G.,Robertson, Jeremy

, p. 7388 - 7394 (2017/09/12)

Application of a modified Du Bois protocol for rhodium-stabilised nitrenoid generation to a variety of allylic carbamates results in 4-acetoxymethyl-1,3-oxazolidin-2-one derivatives with moderate to high levels of stereocontrol.

Metal-free intramolecular aziridination of allylic carbamates mediated by hypervalent iodine compounds

Deng, Qing-Hai,Wang, Jing-Cui,Xu, Zhen-Jiang,Zhou, Cong-Ying,Che, Chi-Ming

, p. 2959 - 2967 (2011/10/19)

An efficient and practical hypervalent iodine compound mediated metal-free intramolecular aziridination reaction of allylic carbamates was developed. Analytically pure aziridines were obtained in high yields by simple filtration of the reaction mixture. I

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