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32438-29-2

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32438-29-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32438-29-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,4,3 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 32438-29:
(7*3)+(6*2)+(5*4)+(4*3)+(3*8)+(2*2)+(1*9)=102
102 % 10 = 2
So 32438-29-2 is a valid CAS Registry Number.

32438-29-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name S-oct-7-enyl ethanethioate

1.2 Other means of identification

Product number -
Other names Ethanethioic acid,S-7-octen-1-yl ester

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:32438-29-2 SDS

32438-29-2Downstream Products

32438-29-2Relevant articles and documents

Terminally perfluorinated long-chain alkanethiols

Graupe, Michael,Koini, Thomas,Wang, Vincent Y.,Nassif, George M.,Colorado Jr, Ramon,Villazana, Ramon J.,Dong, Henry,Miura, Yasuhiro F.,Shmakova, Olga E.,Lee, T. Randall

, p. 107 - 115 (1999)

This paper describes the synthesis of a series of alkanethiols containing perfluorinated terminal segments: F(CF2)m(CH2)nSH, where m = 1, n = 9-15; m = 2, n = 11-14; m = 3, n = 10-13; and m = 4, n = 9-12. Fluorinated alkyl iodides of the general formula F(CF2)m(CH2)nI, where m = 1-4 and n = 0 or 1, were added to long-chain ω-olefins that were functionalized at the α-terminus with a thioacetate group. The reactions proceeded in good yields under free radical conditions. Reduction of the resulting secondary iodides gave long-chain alkanethioacetates with perfluoroalkyl terminal segments. These intermediates were readily transformed into the corresponding terminally perfluorinated alkanethiols by acidic deprotection. The product thiols should find use in the generation of well-defined fluorinated interfaces using the self-assembled monolayer (SAM) technique.

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