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74483-17-3

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74483-17-3 Usage

Use as a reagent

Organic synthesis, particularly in the preparation of phosphine metal complexes

Use as a building block

Various organic chemical reactions

Role of trimethylsilyl group

Protects and stabilizes the phosphine, allowing for greater control and selectivity in its reactions

Potential applications

Pharmaceuticals and agrochemicals

Check Digit Verification of cas no

The CAS Registry Mumber 74483-17-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,4,8 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 74483-17:
(7*7)+(6*4)+(5*4)+(4*8)+(3*3)+(2*1)+(1*7)=143
143 % 10 = 3
So 74483-17-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H14ClPSi/c1-13(2,3)10(12-11)9-7-5-4-6-8-9/h4-8H,1-3H3

74483-17-3SDS

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 chloro-[phenyl(trimethylsilyl)methylidene]phosphane

1.2 Other means of identification

Product number -
Other names 1-Chloro-2-phenyl-2-trimethylsilyl-1-phosphaethen

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:74483-17-3 SDS

74483-17-3Relevant articles and documents

Low Coordinated Phosphorus Compounds, 30 - 1-Chloro-2-phenyl-2-(trimethylsilyl)-1-phosphaethene as a Structural Part for New Phosphaalkenes

Appel, Rolf,Kuendgen, Ursula,Knoch, Falk

, p. 1352 - 1370 (2007/10/02)

New phosphorus-substituted phosphaalkenes are synthesized via a reaction of 1-chloro-2-phenyl-2-(trimethylsilyl)-1-phosphaethene (1) with alcohols, amines, amides, phosphanes, and organometallic reagents.Their structures are well documented by NMR data and in the case of compounds 3a, 5a, and 13 also by an X-ray analysis.Properties and some reactions of the new compounds are given.

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