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Carbamimidic acid, hydroxy-, phenyl ester, monohydrochloride is a complex organic compound with the chemical formula C7H8ClN2O2. It is derived from carbamimidic acid, which is a functional group containing an amide and an isocyanate group. The hydroxy-phenyl ester variant features a hydroxyl group and a phenyl ring attached to the carbamimidic acid structure. The monohydrochloride form indicates the presence of a single hydrogen chloride molecule, which imparts a positive charge to the compound. This chemical is primarily used in the synthesis of pharmaceuticals and other organic compounds, serving as an intermediate in various chemical reactions. Its specific applications may include the production of certain drugs, agrochemicals, or other specialty chemicals, highlighting its importance in the field of organic synthesis.

3174-89-8

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3174-89-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3174-89-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,7 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3174-89:
(6*3)+(5*1)+(4*7)+(3*4)+(2*8)+(1*9)=88
88 % 10 = 8
So 3174-89-8 is a valid CAS Registry Number.

3174-89-8SDS

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 N-hydroxyl-O-phenylisourea hydrochloride

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:3174-89-8 SDS

3174-89-8Relevant academic research and scientific papers

Phenoxychlorocarbene, a Second Ambiphile

Moss, Robert A.,Perez, Leon A.,Wlostowska, Joanna,Guo, Wenjeng,Krogh-Jespersen, Karsten

, p. 4177 - 4180 (2007/10/02)

Phenoxychlorocarbene (PhOCCl) was generated by thermolysis (25 deg C) of 3-chloro-3-phenoxydiazirine and added to six alkenes, affording the corresponding cyclopropanes.The substrates and (relative) reactivities were tetramethylethylene (3.0), isobutene (

Phenoxyoxadiazole cyclopropane carboxylates as insecticides

-

, (2008/06/13)

Compounds of the formula STR1 in which R is methyl, chlorine or bromine and Y is hydrogen or methyl, useful as insecticides.

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