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Propan-2-yl (2,4-dimethylphenyl)carbamate is a chemical compound with the molecular formula C12H17NO2. It is an ester derivative of carbamic acid, where the hydroxyl group is replaced by a propyl group and a 2,4-dimethylphenyl group. propan-2-yl (2,4-dimethylphenyl)carbamate is characterized by its aromatic structure, with two methyl groups attached to the phenyl ring at the 2nd and 4th carbon positions, which can influence its physical and chemical properties. It is a white crystalline solid and is used in various applications, including as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Due to its reactivity and potential applications, it is important to handle propan-2-yl (2,4-dimethylphenyl)carbamate with care, following appropriate safety protocols.

6622-37-3

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6622-37-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6622-37-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6622-37:
(6*6)+(5*6)+(4*2)+(3*2)+(2*3)+(1*7)=93
93 % 10 = 3
So 6622-37-3 is a valid CAS Registry Number.

6622-37-3SDS

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 isopropyl (2,4-dimethylphenyl)carbamate

1.2 Other means of identification

Product number -
Other names -

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:6622-37-3 SDS

6622-37-3Downstream Products

6622-37-3Relevant academic research and scientific papers

Copper-catalyzed carbonylation of anilines by diisopropyl azodicarboxylate for the synthesis of carbamates

Usman, Muhammad,Ren, Zhi-Hui,Wang, Yao-Yu,Guan, Zheng-Hui

, p. 107542 - 107546 (2016)

A Cu-catalyzed efficient methodology for the direct carbonylation of anilines has been developed. The N-H bond cleavage and N-C bond formation were notably achieved under solvent-free conditions and a variety of carbamates were synthesized from readily available anilines using diisopropyl azodicarboxylate (DIAD) as the carbonylating source.

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