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663-41-2

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663-41-2 Usage

Physical state

Colorless liquid

Odor

Slightly sweet

Usage

Building block in the production of pharmaceuticals, agrochemicals, and specialty chemicals

Reactivity

Highly reactive

Potential use

Organic synthesis due to high electronegativity and functionality

Importance

Intermediate in the production of novel agrochemicals and an important building block for the development of new materials and chemical products

Safety precautions

Toxic and can cause irritation to the skin, eyes, and respiratory system upon exposure

Check Digit Verification of cas no

The CAS Registry Mumber 663-41-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,6 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 663-41:
(5*6)+(4*6)+(3*3)+(2*4)+(1*1)=72
72 % 10 = 2
So 663-41-2 is a valid CAS Registry Number.
InChI:InChI=1/C4F4N2/c5-3(6,1-9)4(7,8)2-10

663-41-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,3,3-tetrafluorobutanedinitrile

1.2 Other means of identification

Product number -
Other names tetrafluorobutanedinitrile

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:663-41-2 SDS

663-41-2Relevant articles and documents

-

Bishop et al.

, p. 1606 (1963)

-

Use of Perfluoroalkylfluorosulfonates for Synthesizing Organofluorine Compounds

Rapkin, A. I.,Zabolot-skikh, V. F.,Kochanov, A. S.,Tiunov, A. V.,Zhirnov, O. M.

, p. 133 - 134 (2007/10/03)

The possibility of using fluorosulfation for synthesizing perfluorovinyl and perfluorodivinyl ethers, and also perfluorocarboxylic and perfluorodicarboxylic acids, has been studied.

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