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16090-53-2

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16090-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16090-53-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,9 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16090-53:
(7*1)+(6*6)+(5*0)+(4*9)+(3*0)+(2*5)+(1*3)=92
92 % 10 = 2
So 16090-53-2 is a valid CAS Registry Number.

16090-53-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,4,4,6,6-hexamethyl-1,3,5-trioxa-2,4,6-trigermacyclohexane

1.2 Other means of identification

Product number -
Other names Dimethylgermaniumoxidtrimer

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:16090-53-2 SDS

16090-53-2Downstream Products

16090-53-2Relevant articles and documents

Ring contraction of 1,2-digermacyclohexa-3,5-dienes initiated by electron transfer reactions with TCNE

Mochida, Kunio,Shimizu, Hiromi,Nanjo, Masato

, p. 1226 - 1227 (2007/10/03)

The thermal reaction of 1,2-digermacyclohexa-3,5-dienes with tetracyanoethylene (TCNE) gave 1-germacyclopenta-2,4-diene as a germylene extrusion compound through a charge-transfer complex. The 1-germacyclopenta-2,4-diene was trapped with TCNE to give 5,5,6,6-tetracyano-7-germanor-bornene.

Thermolyse, pyrolyse et photolyse d'heterocycles germanies et soufres a 4 et 5 chainons: especes intermediaires a germanium doublement lie

Barrau, J.,Rima, G.,El-Amine, M.,Satge, J.

, p. 39 - 50 (2007/10/02)

The thermolysis, pyrolysis and photolysis of thiagermetane , dithiagermolane and thiagermetane dioxide have been studied.Thiagermetane and dithiagermolane decompose leading to various new germylated heterocycles: , and probably proceed by two competitive mechanisms which involve the transient species germaethene , germathione , thiagermirane and thiadigermetane .Pyrolysis of thiagermetane dioxide also involves germaethene and probably a new doubly-bonded germanium species, the germasulfene (by mass spectroscopy), which finally gives germoxanes (Me2GeO)n (n = 3,4).

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