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Silanol, [bromobis(trimethylsilyl)methyl]dimethyl-, 4-methylbenzenesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62182-97-2

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62182-97-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62182-97-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,8 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 62182-97:
(7*6)+(6*2)+(5*1)+(4*8)+(3*2)+(2*9)+(1*7)=122
122 % 10 = 2
So 62182-97-2 is a valid CAS Registry Number.

62182-97-2SDS

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 Brom<dimethyl(p-tolylsulfonyloxy)silyl>bis(trimethylsilyl)methan

1.2 Other means of identification

Product number -
Other names Brom[dimethyl(p-tolylsulfonyloxy)silyl]bis(trimethylsilyl)methan

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:62182-97-2 SDS

62182-97-2Downstream Products

62182-97-2Relevant academic research and scientific papers

On the Way to Silaethene Me2Si=C(SiMe3)2: Trisilylated Methanes (Me3Si)2(Me2XSi)CY (X=e. g. Hal, RO, RS; Y e. g. Br, Li)

Wiberg, Nils,Preiner, Gerhard,Schieda, Oswald

, p. 2087 - 2103 (2007/10/02)

Bromotrisilylmethanes (Me3Si)2(Me2XSi)CBr (1 - 15) are formed as a result of the reaction of (Me3Si)2(Me2PhSi)CBr (16) with iodine monochloride, bromine and iodine (X = Cl, Br, I) respectively, and also through the reaction of (Me3Si)2(Me2BrSi)CBr (1) with AgX (X = F, p-TolSO2, p-TolSO3, MesSO3, Ph2PO2, Ph2PO3, Ph2PO4) or MX (M = H, Li, Na; X = HO, RO, RS, Bu, Ph).Butyl- as well as phenyllithium convert bromotrisilylmethanes 1 - 16 at low temperatures into lithium derivatives (Me3Si)2(Me2XSi)CLi (1a - 16a).These are in some cases (X = R, RO) thermostable, whereas, in other cases they decompose more or less readily under LiX elimination and lead (in many cases via silaethene Me2Si=C(SiMe3)2) to the disilacyclobutane derivative 2 (17).Acids HZ (e. g.HCl, HOMe, Me3CBr) protonate the lithium compounds into (Me3Si)2(Me2XSi)CH as well as (Me3Si)2(Me2ZSi)CH.Butyl bromide converts the more stable lithium compounds (Me3Si)2(Me2XSi)CLi (X = R, RO, F, Ph2POn) into butyl derivatives (Me3Si)2(Me2XSi)CBu.

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