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2621-01-4

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2621-01-4 Usage

Physical state

Clear, colorless liquid

Uses

Reagent in organic synthesis, building block for functionalized silicon compounds, production of functionalized siloxanes, precursor in the synthesis of organosilicon compounds, and synthesis of materials for electronic and semiconductor applications

Reactivity

Highly reactive

Stability

Sensitive to moisture and air, must be handled with caution

Check Digit Verification of cas no

The CAS Registry Mumber 2621-01-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,2 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2621-01:
(6*2)+(5*6)+(4*2)+(3*1)+(2*0)+(1*1)=54
54 % 10 = 4
So 2621-01-4 is a valid CAS Registry Number.
InChI:InChI=1/C3H4Cl3NSi/c1-3(2-7)8(4,5)6/h3H,1H3

2621-01-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-trichlorosilylpropanenitrile

1.2 Other means of identification

Product number -
Other names 2-(Trichlorosilyl)propiononitrile

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:2621-01-4 SDS

2621-01-4Downstream Products

2621-01-4Relevant articles and documents

Reaction of unsaturated nitriles with hydrosilanes

Belyakova,Pomerantseva,Chekrii,Chernyshev,Storozhenko

experimental part, p. 927 - 929 (2011/01/05)

Reaction of acrylonitrile and 1,4-dicyanobut-1-ene with hydrosilanes in the presence of various catalysts was studied. In the presence of triallylamine, allyl-bis(triethoxypropyl)amine, diallylaminopropyltriethoxysilane, HMPA, NiCl2 + 2MePh2PO, CuCl + 2MePh2PO, [(Me 2N)2CCl]2CuCl4, and [(Me 2N)2CCl]2PtCl6, the addition of trichlorosilane to acrylonitrile proceeded with the yield of 36 to 97%. Triethoxy-and tributoxysilane were added to acrylonitrile in the presence of rhodium dicarbonyl acetylacetonate with the formation of α-isomer in 56-58% yield. Attempted addition of hydrosilanes to 1,4-dicyanobutene failed. Pleiades Publishing, Ltd., 2010.

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