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2234-97-1

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2234-97-1 Usage

Chemical Properties

Clear colorless liquid

Uses

suzuki reaction

Check Digit Verification of cas no

The CAS Registry Mumber 2234-97-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,3 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2234-97:
(6*2)+(5*2)+(4*3)+(3*4)+(2*9)+(1*7)=71
71 % 10 = 1
So 2234-97-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H21P/c1-4-7-10(8-5-2)9-6-3/h4-9H2,1-3H3

2234-97-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (H27838)  Tri-n-propylphosphine, 98%   

  • 2234-97-1

  • 5g

  • 837.0CNY

  • Detail
  • Alfa Aesar

  • (H27838)  Tri-n-propylphosphine, 98%   

  • 2234-97-1

  • 25g

  • 2562.0CNY

  • Detail
  • Alfa Aesar

  • (H27838)  Tri-n-propylphosphine, 98%   

  • 2234-97-1

  • 100g

  • 7254.0CNY

  • Detail

2234-97-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name tripropylphosphane

1.2 Other means of identification

Product number -
Other names Tri-propylphosphine

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:2234-97-1 SDS

2234-97-1Relevant articles and documents

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Jensen

, p. 225,250 (1936)

-

Production method of alkyl phosphine (by machine translation)

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Paragraph 0044-0059, (2020/12/10)

The method comprises the following steps: mixing phosphine and propylene in a solvent, then adding the photocatalyst, reacting the phosphine with propylene in 20 - 50W light irradiation, and having short reaction time, relatively simple reaction time, relatively simple post-treatment, relatively simple post-treatment, and higher yield and purity of the product compared with the prior art, and the reaction time is shorter. 1 - 12h 0 °C - 50 °C. The method comprises the following steps of: carrying out free radical reaction at a temperature and a normal pressure. (by machine translation)

Method for manufacturing acryloxypropysilane

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, (2008/06/13)

A method to manufacture acryloxypropylsilane to a high degree of purity is achieved by hydrosilation of (A) allyl acrylate or allyl methacrylate by (B) a hydrosilane compound, using (C) a platinum-containing compound as the catalyst and (D) an organic phosphorus compound as the promoter. The acryloxypropylsilane product is expressed by General Formula I where R1 represents a hydrogen or methyl group, R2 represents a hydrolyzable group, R3 represents an aryl, alkenyl or aryl group of carbon number 1-12, and n is 0, 1, 2, or 3.

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