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18269-50-6

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18269-50-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18269-50-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,6 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 18269-50:
(7*1)+(6*8)+(5*2)+(4*6)+(3*9)+(2*5)+(1*0)=126
126 % 10 = 6
So 18269-50-6 is a valid CAS Registry Number.

18269-50-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (isopropylmethoxy)trimethylsilane

1.2 Other means of identification

Product number -
Other names Isobutoxy-trimethyl-silan

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:18269-50-6 SDS

18269-50-6Relevant articles and documents

New methods of synthesis of boron, germanium, and tin derivatives of pentavalent phosphorus thioacids

Nizamov, Il'yas S.,Sorokina, Tat'yana P.,Nizamov, Il'nar D.,Galimullina, Nailya G.,Batyeva, Elvira S.,Alfonsov, Vladimir A.

, p. 27 - 35 (2007/10/03)

The reaction of S-trimethysilyl esters of S-propyl-4-methoxyphenyltrithiophosphonic, bis-(dialkylamido)dithiophosphoric, and S-ethyl-diethylamidotrithiophosphoric acid with trialkyl borates, triorganylbromogermanes, trimethyl(isobutylthio)germane, and tri

The mechanism of the formation of silyl enol ethers from hydrosilanes and organic carbonyl compounds in the presence of cobalt carbonyls. Kinetic investigation of some reaction steps

Kovács, István,Sisak, Attila,Ungváry, Ferenc,Markó, László

, p. 1025 - 1028 (2008/10/08)

The cleavage of isobutyrylcobalt tetracarbonyl with triethylsilane gives (triethylsilyl)cobalt tetracarbonyl, isobutyraldehyde, dicobalt octacarbonyl, and the corresponding unsaturated and saturated silyl ethers. Silyl enol ether was also formed, along wi

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