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24929-99-5

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24929-99-5 Usage

General Description

Trimethylsilyl 2,2,3,3,4,4,4-heptafluorobutanoate is a compound used in organic synthesis as a protecting group for alcohols. It is commonly used in the modification of organic compounds to enhance their stability and reactivity. This chemical is known for its ability to protect functional groups during various chemical reactions and is particularly useful in the production of pharmaceuticals and agrochemicals. Trimethylsilyl 2,2,3,3,4,4,4-heptafluorobutanoate is a versatile compound with a wide range of applications in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 24929-99-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,9,2 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24929-99:
(7*2)+(6*4)+(5*9)+(4*2)+(3*9)+(2*9)+(1*9)=145
145 % 10 = 5
So 24929-99-5 is a valid CAS Registry Number.

24929-99-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name heptafluorobutyrate trimethylsilyl ester

1.2 Other means of identification

Product number -
Other names TRIMETHYLSILYL HEPTAFLUOROBUTANOATE

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:24929-99-5 SDS

24929-99-5Downstream Products

24929-99-5Relevant articles and documents

Perfluorocarboxylato disulfides and methylsilanes

Wang, Charlene S.,Pullen, Kent E.,Shreeve, Jean'ne M.

, p. 90 - 92 (1970)

The reaction of disulfur dichloride, S2Cl2, with silver perfluorocarboxylates gives substituted disulfides, (RfCO2S)2, where Rf = CF3, C2F5, C3F

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