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Carbonochloridic acid, 3-(trichloromethyl)phenyl ester, also known as 3-(trichloromethyl)phenyl chloroformate, is an organic compound with the chemical formula C8H3Cl4O2. It is a colorless liquid that is sensitive to light and heat, and it decomposes upon exposure to air. Carbonochloridic acid, 3-(trichloromethyl)phenyl ester is a derivative of carbonochloridic acid, where the hydroxyl group is replaced by a 3-(trichloromethyl)phenyl group. It is used as a reagent in organic synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals. Due to its reactivity and potential toxicity, it is important to handle this chemical with care, following proper safety protocols.

713-94-0

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713-94-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 713-94-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 713-94:
(5*7)+(4*1)+(3*3)+(2*9)+(1*4)=70
70 % 10 = 0
So 713-94-0 is a valid CAS Registry Number.

713-94-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-(trichloromethyl)phenyl] carbonochloridate

1.2 Other means of identification

Product number -
Other names Chlorameisensaeure-<3-trichlormethyl-phenylester>

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:713-94-0 SDS

713-94-0Upstream product

713-94-0Relevant academic research and scientific papers

Process for preparing hydroxylated aromatic compounds

-

, (2008/06/13)

A process for preparing hydroxylated aromatic compounds optionally bearing at least one trifluoromethyl, trifluoromethoxy or trifluoromethylthio group. A chloroformate or fluoroformate, optionally bearing at least one trihalomethyl-, trihalomethoxy- or trihalomethylthiophenyl group, is reacted with liquid hydrofluoric acid. The aromatic compounds obtained are useful as synthesis intermediates in the pharmaceutical or the plant-protection industry.

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