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10335-98-5

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10335-98-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10335-98-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,3 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10335-98:
(7*1)+(6*0)+(5*3)+(4*3)+(3*5)+(2*9)+(1*8)=75
75 % 10 = 5
So 10335-98-5 is a valid CAS Registry Number.

10335-98-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,2-Dimethyl-propyl)-phenyl-sulfoxid

1.2 Other means of identification

Product number -
Other names Neopentyl-phenyl-sulfoxid

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:10335-98-5 SDS

10335-98-5Relevant articles and documents

Sulfoxide and Sulfone Synthesis via Electrochemical Oxidation of Sulfides

Lee, Sunwoo,Park, Jin Kyu

, p. 13790 - 13799 (2021/10/12)

The oxidation of diaryl sulfides and aryl alkyl sulfides to the corresponding sulfoxides and sulfones under electrochemical conditions is reported. Sulfoxides are selectively obtained in good yield under a constant current of 5 mA for 10 h in DMF, while sulfones are formed as the major product under a constant current of 10 or 20 mA for 10 h in MeOH. The oxygen of both the sulfoxide and sulfone function is derived from water.

Diastereoselective radical alkylations of alkyl aryl sulfoxides

Zahouily, Mohamed,Caron, Giulia,Carrupt, Pierre-Alain,Knouzi, Nourdine,Renaud, Philippe

, p. 8387 - 8390 (2007/10/03)

1,2-Asymmetric induction in reactions of arylsulfinylated radicals has been examined and compared to the anionic processes. A rule of thumb allowing to predict the stereoselectivity is presented.

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