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Para-(trichloromethyl)benzene isocyanate, also known as TCPB-isocyanate, is a chemical compound with the molecular formula C9H6Cl3NO. It is a derivative of benzene, where one hydrogen atom is replaced by an isocyanate group (-NCO) and another hydrogen atom is replaced by a trichloromethyl group (CCl3). para-(trichloromethyl)benzene isocyanate is characterized by its reactivity and is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its high reactivity, it is important to handle para-(trichloromethyl)benzene isocyanate with care, as it can be hazardous and may cause irritation or other health effects if not properly managed.

709-66-0

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709-66-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 709-66-0 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 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 709-66:
(5*7)+(4*0)+(3*9)+(2*6)+(1*6)=80
80 % 10 = 0
So 709-66-0 is a valid CAS Registry Number.

709-66-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name para-(trichloromethyl)benzene isocyanate

1.2 Other means of identification

Product number -
Other names p-trichloromethylphenyl isocyanate

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:709-66-0 SDS

709-66-0Relevant academic research and scientific papers

Process for the halogenation, nitration and fluorination of aromatic derivatives

-

, (2008/06/13)

A process for the halogenation (bromination or chlorination)/nitration/fluorination of aromatic derivatives substituted by at least one group containing a halogenoalkyl unit. The aromatic derivative is reacted with a halogen and a nitrating agent in liquid hydrofluoric acid. The products obtained are useful as intermediates for the synthesis of compounds having a plant-protecting or pharmaceutical activity.

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