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18395-92-1

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18395-92-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18395-92-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,9 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 18395-92:
(7*1)+(6*8)+(5*3)+(4*9)+(3*5)+(2*9)+(1*2)=141
141 % 10 = 1
So 18395-92-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H18Cl2Si/c1-7(2)5-11(9,10)6-8(3)4/h7-8H,5-6H2,1-4H3

18395-92-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name dichloro-bis(2-methylpropyl)silane

1.2 Other means of identification

Product number -
Other names Silane,dichlorodiisobutyl

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:18395-92-1 SDS

18395-92-1Downstream Products

18395-92-1Relevant articles and documents

One-pot condensation of a bicyclo[1.1.1]pentasilane through elimination of iodotrimethylsilane assisted by a lewis base

Yokouchi, Yuki,Iwamoto, Takeaki

, p. 3301 - 3305 (2020)

Development of efficient bond formation reactions remains important in organic and main-group-element chemistry. Herein, we report the metal-free one-pot condensation reaction of 1-iodo-3-trimethylsilyl-substituted bicyclo[1.1.1]pentasilane (BPS) in the presence of 4-(dimethylamino)pyridine (DMAP) providing oligomers of BPS, persila[n]staffanes (n = 2, 3), which involves the successive Si?Si bond formation reaction accompanied by the concomitant formation of iodotrimethylsilane (TMSI) in the form of a DMAP complex. The computational study suggests that the formation of a pentasila[1.1.1]propellane?DMAP complex resulting from the elimination of TMSI from the BPS is a key intermediate.

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