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4342-30-7

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4342-30-7 Usage

Hazard

A poison by ingestion. Tributyl tin com- pounds are extremely toxic to marine life.

Check Digit Verification of cas no

The CAS Registry Mumber 4342-30-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,4 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4342-30:
(6*4)+(5*3)+(4*4)+(3*2)+(2*3)+(1*0)=67
67 % 10 = 7
So 4342-30-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H6O3.3C4H9.Sn/c8-6-4-2-1-3-5(6)7(9)10;3*1-3-4-2;/h1-4,8H,(H,9,10);3*1,3-4H2,2H3;/rC12H27Sn.C7H6O3/c1-4-7-10-13(11-8-5-2)12-9-6-3;8-6-4-2-1-3-5(6)7(9)10/h4-12H2,1-3H3;1-4,8H,(H,9,10)

4342-30-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name tributylstannyl 2-hydroxybenzoate

1.2 Other means of identification

Product number -
Other names Tributylstannyl salicylate

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:4342-30-7 SDS

4342-30-7Downstream Products

4342-30-7Relevant articles and documents

N-Heterocyclic carbene catalyzed oxidative stannylation of aldehydes: A facile entry to organotin(IV) carboxylates

Reddi, Rambabu N.,Malekar, Pushpa V.,Sudalai, Arumugam

, p. 2679 - 2681 (2013/06/05)

A simple protocol is described for the oxidative transformation of aldehydes to the corresponding organotin(IV) carboxylates in high yields (up to 90%) that utilizes atmospheric O2 as the sole oxidant, N-heterocyclic carbene as catalyst (at 10 mol %), and tributyl tin chloride as stannylating agent. The uniqueness of the reaction lies in the direct conversion of aldehydes to the corresponding organotin(IV) carboxylates via stannylation of carboxylic acids, generated from the reaction of a Breslow intermediate with O2.

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