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2975-46-4

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2975-46-4 Usage

Uses

3-Trimethylsilylpropynal acts as an important organic intermediate. It is used in agrochemicals, pharmaceuticals and dyestuff field. Further, it is used in the preparation of [3-(trimethylsilyl)-2-propinyliden]-malononitrile.

Check Digit Verification of cas no

The CAS Registry Mumber 2975-46-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,7 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2975-46:
(6*2)+(5*9)+(4*7)+(3*5)+(2*4)+(1*6)=114
114 % 10 = 4
So 2975-46-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H10OSi/c1-8(2,3)6-4-5-7/h5H,1-3H3

2975-46-4 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (44763)  3-Trimethylsilylpropynal, 97%   

  • 2975-46-4

  • 0.25g

  • 347.0CNY

  • Detail
  • Alfa Aesar

  • (44763)  3-Trimethylsilylpropynal, 97%   

  • 2975-46-4

  • 1g

  • 1088.0CNY

  • Detail
  • Alfa Aesar

  • (44763)  3-Trimethylsilylpropynal, 97%   

  • 2975-46-4

  • 5g

  • 4332.0CNY

  • Detail

2975-46-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-trimethylsilylprop-2-ynal

1.2 Other means of identification

Product number -
Other names trimethylsilylprop-2-yn-1-al

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:2975-46-4 SDS

2975-46-4Relevant articles and documents

Reactivity of indole-3-alkoxides in the absence of acids: Rapid synthesis of homo-bisindolylmethanes

Chinta, Bhavani Shankar,Baire, Beeraiah

, p. 8106 - 8116 (2016/11/22)

An unprecedented behaviour of in situ generated indole-3-alkoxides (MgX or Li) has been reported. Tuning the electronic properties of the alkoxides offered the direct and selective construction of bisindolylmethanes and indole-3-carbinols. This process shows very broad scope and represents the reagent (external) free, greener synthesis of structurally divergent bisindolylmethanes.

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