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Phenylcarbamic acid cyclopentyl ester, also known as cyclopentyl phenylcarbamate, is an organic compound with the chemical formula C12H15NO2. It is a derivative of phenylcarbamic acid, where the hydroxyl group is replaced by a cyclopentyl group. This ester is a colorless to pale yellow liquid with a molecular weight of 205.25 g/mol. It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of herbicides and insecticides. The compound is characterized by its reactivity, as it can undergo hydrolysis to regenerate phenylcarbamic acid or participate in other chemical reactions. It is typically handled with care due to its potential toxicity and is stored under controlled conditions to maintain stability.

3422-04-6

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3422-04-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3422-04-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,2 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3422-04:
(6*3)+(5*4)+(4*2)+(3*2)+(2*0)+(1*4)=56
56 % 10 = 6
So 3422-04-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H15NO2/c14-12(15-11-8-4-5-9-11)13-10-6-2-1-3-7-10/h1-3,6-7,11H,4-5,8-9H2,(H,13,14)

3422-04-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclopentyl N-phenylcarbamate

1.2 Other means of identification

Product number -
Other names O-Cyclopentyl-N-phenyl-urethan

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:3422-04-6 SDS

3422-04-6Downstream Products

3422-04-6Relevant academic research and scientific papers

Metal free oxidative coupling of aryl formamides with alcohols for the synthesis of carbamates

Reddy, N. Veera,Prasad, K. Rajendra,Reddy, P. Sudhir,Lakshmi Kantam,Reddy, K. Rajender

supporting information, p. 2172 - 2175 (2014/04/03)

A direct transformation of N-aryl formamides to the corresponding carbamates via the formation of isocyanate intermediates is achieved in good yields using hypervalent iodine as an oxidant. This journal is

2-chloro-1,3-dimethylimidazolinium chloride. 3. Utility for chlorination, oxidation, reduction, and rearrangement reactions

Isobe, Toshio,Ishikawa, Tsutomu

, p. 5832 - 5835 (2007/10/03)

2-Chloro-1,3-dimethylimidazolinium chloride (1), which can act as a powerful dehydrating equivalent to DCC (2), is also applicable to chlorination, oxidation, reduction, and rearrangement under nearly neutral conditions. The utility of 1 for these reactions is described.

A CONVENIENT LEWIS ACID CATALYZED PREPARATION OF CARBAMATES FROM SECONDARY ALKOHOLS AND ISOCYANATES

Ibuka, Toshiro,Chu, Gil-Namg,Aoyagi, Takeshi,Kitada, Kazuko,Tsukida, Takahiro,Yoneda, Fumio

, p. 451 - 454 (2007/10/02)

The Lewis acids have been found to be highly effective catalysts for the carbamate formation from secondary alcohols and isocyanates.KEYWORDS - Lewis acid; secondary alcohol; isocyanate; carbamate; γ-carbamoyloxy-α,β-enoate

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