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40200-59-7

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40200-59-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40200-59-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,2,0 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 40200-59:
(7*4)+(6*0)+(5*2)+(4*0)+(3*0)+(2*5)+(1*9)=57
57 % 10 = 7
So 40200-59-7 is a valid CAS Registry Number.

40200-59-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name propylphosphane

1.2 Other means of identification

Product number -
Other names propyl-phosphine

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:40200-59-7 SDS

40200-59-7Downstream Products

40200-59-7Relevant articles and documents

Partheil,Gronover

, p. 411 (1903)

Preparation of primary and secondary alkyl phosphines from elemental phosphorus or phosphorus trichloride in organic solvents

Van Hooijdonk,Gerritsen,Brandsma

, p. 39 - 49 (2007/10/03)

A number of volatile and non-volatile primary and secondary alkyl phosphines have been prepared by one-pot procedures from elemental phosphorus or from phosphorus trichloride. The element or chloride was first converted into trisodium phosphide by reaction with sodium in the presence of naphthalene or another solubilisation reagent. Subsequent addition of two equivalents of t-butyl alcohol and an alkyl halide gave monoalkyl phosphines in fair to good yields. In situ conversion of the primary phosphine into a dialkyl phosphine was achieved by metallation with BuLi or sodium and subsequent alkylation.

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