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15239-22-2

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15239-22-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15239-22-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,3 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15239-22:
(7*1)+(6*5)+(5*2)+(4*3)+(3*9)+(2*2)+(1*2)=92
92 % 10 = 2
So 15239-22-2 is a valid CAS Registry Number.

15239-22-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethylstannyl 2-chloroacetate

1.2 Other means of identification

Product number -
Other names Monochloressigsaeure-trimethylstannylester

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:15239-22-2 SDS

15239-22-2Downstream Products

15239-22-2Relevant articles and documents

The β-effect with vinyl cations: Kinetic study of the protiodemetalation of silyl-, germyl-, and stannylalkynes

Dallaire, Carol,Brook, Michael A.

, p. 2332 - 2338 (2008/10/08)

The relative magnitude of the hyperconjugative stabilization of vinyl cations by adjacent C-M bonds (M = Si, Ge, Sn; the β-effect) has been examined by measuring the rate constants for the protonation and subsequent protiodemetalation of group 14 metalated (trimethylsilyl)-acetylenes (R3MC≡CSiMe3). The relative β-effect arising from the second-order rate constants Sn ? Ge > Si (maximum kM/kSi = 108, 5 × 102, 1, respectively) follows the same order as that reported for simple carbenium ions. The product ratio from the protonation of Ph3GeC≡CSiMe3 was found to be particularly sensitive to acid concentration and strength, leading to loss of Ph3Ge preferentially with weaker acids. With tin groups, the rate of destannylation decreased with increasing steric bulk, unlike the corresponding situation with silyl groups. The origins of both these observations may be attributed to nucleophilic interaction at the metal center during protonation.

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