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496045-96-6

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496045-96-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 496045-96-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,6,0,4 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 496045-96:
(8*4)+(7*9)+(6*6)+(5*0)+(4*4)+(3*5)+(2*9)+(1*6)=186
186 % 10 = 6
So 496045-96-6 is a valid CAS Registry Number.

496045-96-6SDS

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-[bis(ethylsulfanyl)methyl]-2-nitrobenzene

1.2 Other means of identification

Product number -
Other names 2-nitrobenzaldehyde diethylthioacetal

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:496045-96-6 SDS

496045-96-6Downstream Products

496045-96-6Relevant articles and documents

Simple, mild and efficient thioacetalization and transthioacetalization of carbonyl compounds and deprotection of thioacetals: Unique role of thiols in the selectivity of thioacetalization

Das, Biswanath,Ramu, Ravirala,Reddy, Majjigapu Ravinder,Mahender, Gurram

, p. 250 - 254 (2007/10/03)

Silica supported sodium hydrogen sulfate (NaHSO4·SiO 2) has been employed for efficient thioacetalization and transthioacetalization of carbonyl compounds in CH2Cl2 at room temperature. Selectivity of thioacetalization was dependent on the thiols used for the conversion. The same catalyst was also found to be effective for deprotection of thioacetals in CH2Cl2-H2O at room temperature.

Oxathioacetalization, thioacetalization and transthioacetalization of carbonyl compounds by N-bromosuccinimide: Selectivity and scope

Kamal, Ahmed,Chouhan, Gagan,Ahmed, Kaleem

, p. 6947 - 6951 (2007/10/03)

Efficient oxathioacetalization, thioacetalization and transthioacetalization of carbonyl compounds have been achieved in high yields employing N-bromosuccinimide as a catalyst.

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