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Cyclohexanemethanol, 1-carbamate, also known as 1-(hydroxymethyl)cyclohexanecarbamate, is a chemical compound with the molecular formula C8H15NO2. It is a colorless liquid with a density of 1.06 g/cm3 and a boiling point of 250°C. Cyclohexanemethanol,1-carbamate is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, other and organic compounds. It is also known for its potential applications in the production of insecticides and herbicides. Due to its reactivity, it is essential to handle this chemical with proper safety measures, including the use of personal protective equipment and proper ventilation.

6629-35-2

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6629-35-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6629-35-2 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 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6629-35:
(6*6)+(5*6)+(4*2)+(3*9)+(2*3)+(1*5)=112
112 % 10 = 2
So 6629-35-2 is a valid CAS Registry Number.

6629-35-2SDS

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 [(1R,2S,5R)-5-methyl-2-propan-2-ylcyclohexyl] (2S)-5-oxopyrrolidine-2-carboxylate

1.2 Other means of identification

Product number -
Other names 1-Carbamoyloxy-2-(2-methyl-butoxy)-aethan

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:6629-35-2 SDS

6629-35-2Relevant academic research and scientific papers

Iron-catalyzed reaction of urea with alcohols and amines: A safe alternative for the synthesis of primary carbamates

Pe?a-López, Miguel,Neumann, Helfried,Beller, Matthias

, p. 2233 - 2238 (2017/07/25)

A general study of the iron-catalyzed reaction of urea with nucleophiles is here presented. The carbamoylation of alcohols allows for the synthesis of N-unsubstituted (primary) carbamates, including present drugs (Felbamate and Meprobamat, without the necessity to apply phosgene and related derivatives. Using amines as nucleophiles gave rise to the respective mono-and disubstituted ureas via selective transamidation reaction. These atom-economical transformations provide a direct and selective access to valuable compounds from cheap and readily available urea using a simple Lewis-acidic iron(Icatalyst.

Copper-catalyzed intramolecular C-H amination

Barman, Dipti N.,Nicholas, Kenneth M.

, p. 908 - 911 (2011/04/26)

The amino-functionalization of tertiary, secondary and benzylic C-H bonds of tethered carbamates and sulfamates by iodosobenzene is catalyzed by Cu I-diimine complexes in moderate to good yield. Employing homochiral imine-Cucatalysts affords oxazolidinones and oxathiazinanes with modest enantioselectivity.

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