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Pentyl hydroxycarbamate, also known as N-hydroxy-N-pentylcarbamate, is an organic compound with the chemical formula C6H13NO2. It is a derivative of hydroxycarbamic acid, where the hydrogen atom is replaced by a pentyl group (a five-carbon alkyl chain). pentyl hydroxycarbamate is used as a precursor in the synthesis of various carbamates, which are important in the production of pharmaceuticals, pesticides, and other chemicals. Pentyl hydroxycarbamate is a colorless liquid with a mild, characteristic odor and is soluble in organic solvents. It is sensitive to heat and moisture, and its stability can be affected by exposure to light and air. Due to its reactivity, it is typically handled and stored under controlled conditions to prevent decomposition or unwanted reactions.

590-06-7

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590-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 590-06-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 590-06:
(5*5)+(4*9)+(3*0)+(2*0)+(1*6)=67
67 % 10 = 7
So 590-06-7 is a valid CAS Registry Number.

590-06-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name pentyl N-hydroxycarbamate

1.2 Other means of identification

Product number -
Other names Hydroxycarbamic acid pentyl 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:590-06-7 SDS

590-06-7Downstream Products

590-06-7Relevant academic research and scientific papers

Regioselective Synthesis of 2-Vinylanilines Using O-aroyloxycarba-mates by Sequential Decarboxylation/Amination/Heck Reaction

Li, Peihe,Ma, Nuannuan,Li, Jikun,Wang, Zheng,Dai, Qipu,Hu, Changwen

, p. 8251 - 8257 (2017/08/14)

A new sequential approach for 2-vinylanilines utilizing aryl carboxylic acids as stable, inexpensive and widely available arylating reagents is described. Employing a Pd-POVs catalyst system, this protocol is not only overcoming the restriction barrier of decarboxylative coupling to ortho-substituted substrates, but also provides site-special to create new C(sp2)-N and C(sp2)-C(sp2) bonds. Mechanistic experiments suggest the cleavage of C(sp2)-COOH gives priority to C(sp2)-X bond in this reaction.

Palladium-Catalyzed Decarboxylative Synthesis of Arylamines

Dai, Qipu,Li, Peihe,Ma, Nuannuan,Hu, Changwen

supporting information, p. 5560 - 5563 (2016/11/17)

A novel approach has been developed for the synthesis of arylamines via the palladium-catalyzed intramolecular decarboxylative coupling (IDC) of aroyloxycarbamates, obtained in situ by reacting aryl carboxylic acids with hydroxycarbamates. The reaction offers facile access to structurally diverse arylamines with the site-specific formation of the C(sp2)-N bond under mild conditions.

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