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16054-12-9

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16054-12-9 Usage

Physical state

Colorless liquid

Boiling point

34-35°C

Solubility

Insoluble in water

Usage

Building block in organic synthesis

Usage

Precursor in the production of other organosilicon compounds

Structural feature

Unique silole structure

Property

High thermal stability

Applications

Materials science

Applications

Electronics

Applications

Pharmaceuticals

Reactivity

Highly reactive

Safety

Must be handled with care in a controlled environment

Safety

Potential hazards if not properly managed

Check Digit Verification of cas no

The CAS Registry Mumber 16054-12-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,5 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16054-12:
(7*1)+(6*6)+(5*0)+(4*5)+(3*4)+(2*1)+(1*2)=79
79 % 10 = 9
So 16054-12-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H12Si/c1-7(2)5-3-4-6-7/h3-4H,5-6H2,1-2H3

16054-12-9SDS

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 1,1-dimethyl-2,5-dihydrosilole

1.2 Other means of identification

Product number -
Other names 1,1-dimethyl-1-silacyclopent-3-ene

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:16054-12-9 SDS

16054-12-9Relevant articles and documents

Unprecedented effects of the trimethylsilyl group on the reactivity of 3C-silylated silacyclopentenes and their derivatives

Boukherroub, Rabah,Manuel, Georges

, p. 141 - 149 (2007/10/03)

We have synthesised new 3C-silylated silacyclopentenes from the corresponding 3-trimethylsilyl-1,1-dichloro-1-silacyclopent-3-enes. The presence of two metal centres M (M = Si) in α and β-positions confers an original structure for these new heterocycles. The chemical behaviour of such compounds and their derivatives was studied and compared to the results obtained in the non-substituted silacyclopentane series.

Kinetics of the Isomerization of 1-Methylsilene to Dimethylsilylene

Conlin, Robert T.,Kwak, Young-Woo

, p. 834 - 835 (2007/10/02)

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MISE EN EVIDENCE DE LA FORMATION DE R2M=MR2 A PARTIR DE DISILA-1,2 ET DIGERMA-1,2 CYCLOHEXENES-4

Marchand, Annette,Gerval, Pierre,Duboudin, Francoise,Gaufryau, M.-H.,Joanny, Marguerite,Mazerolles, Pierre

, p. 93 - 106 (2007/10/02)

Intermediates with ?-bonded Si or Ge are generated during gas phase pyrolysis of 1,2-disila- or 1,2-digerma-cyclohex-4-enes. Compounds such as R2M=MR2 are successfully trapped by addition or and cycloadditions.These results were proved by mass spectrometry.

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