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1-Propanol, 3-[dimethyl(phenylmethyl)silyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61676-43-5

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61676-43-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61676-43-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,7 and 6 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 61676-43:
(7*6)+(6*1)+(5*6)+(4*7)+(3*6)+(2*4)+(1*3)=135
135 % 10 = 5
So 61676-43-5 is a valid CAS Registry Number.

61676-43-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[benzyl(dimethyl)silyl]propan-1-ol

1.2 Other means of identification

Product number -
Other names -

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:61676-43-5 SDS

61676-43-5Relevant academic research and scientific papers

Rearrangements of α-Halosilanes Induced by Intramolecular Nucleophilic Attack at Silicon

Hudrlik, Paul F.,Abdallah, Yousef M.,Hudrlik, Anne M.

, p. 6743 - 6746 (2007/10/02)

Migrations of organic groups from silicon to carbon are facilitated by intramolecular attack by alkoxide at silicon.

BASE CLEAVAGE OF THE BENZYL-SILICON BOND IN PhCH2SiMe2(CH2)nOH (n = 2 or 3) COMPOUNDS

Eaborn, Colin,Mahmoud, Foad M.S.

, p. 13 - 16 (2007/10/02)

The compounds PhCH2SiMe2(CH2)nOH with n = 2 or 3 are cleaved 0.75 and 95-135 times, respectively, as readily as PhCH2SiMe3 by NaOMe/MeOH at 50 deg C.The high reactivity of the compound with n = 3 may arise from intramolecular attack of the alkoxide centre

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