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Phenol, 4-fluoro-, methylcarbamate, also known as 4-fluorophenol methylcarbamate, is a chemical compound with the molecular formula C8H8FNO2. It is a derivative of phenol, where one of the hydrogen atoms on the phenol ring is replaced by a fluorine atom, and a methylcarbamate group is attached to the remaining hydroxyl group. Phenol, 4-fluoro-, methylcarbamate is an organic compound that belongs to the class of carbamates, which are known for their use as pesticides and pharmaceuticals. It is characterized by its potential reactivity and the presence of a fluorine atom, which can significantly alter the chemical properties and reactivity compared to its non-fluorinated counterparts. The specific applications and hazards of Phenol, 4-fluoro-, methylcarbamate would depend on its intended use and the context in which it is being considered.

705-70-4

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705-70-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 705-70-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 705-70:
(5*7)+(4*0)+(3*5)+(2*7)+(1*0)=64
64 % 10 = 4
So 705-70-4 is a valid CAS Registry Number.

705-70-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-fluorophenol,methylcarbamic acid

1.2 Other means of identification

Product number -
Other names p-Fluorphenylmethylcarbamat

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:705-70-4 SDS

705-70-4Downstream Products

705-70-4Relevant academic research and scientific papers

A non-MIC route to carbamates: Irreversible trans-esterification reaction of methyl N-methylcarbamate with phenolic substrates possessing additional functional groups

Kumaran, G.,Naik, R. H.,Kulkarni, G. H.

, p. 893 - 895 (2007/10/02)

The novel non-MIC route to aryl carbamates, involving irreversible trans-esterification of methyl N-methylcarbamate has been carried out on a variety of phenolic substrates possessing additional functional groups for studying the scope of the reaction.The carbamates, thus synthesised, have been screened for their insecticidal activity against Musca domestica.

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