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50766-69-3

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50766-69-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50766-69-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,7,6 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 50766-69:
(7*5)+(6*0)+(5*7)+(4*6)+(3*6)+(2*6)+(1*9)=133
133 % 10 = 3
So 50766-69-3 is a valid CAS Registry Number.

50766-69-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-methoxy-4-phenylmethoxyphenyl)-1,3-dithiane

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:50766-69-3 SDS

50766-69-3Relevant articles and documents

Yttrium triflate as an efficient and useful catalyst for chemoselective protection of carbonyl compounds

De, Surya Kanta

, p. 2339 - 2341 (2007/10/03)

Carbonyl compounds have been successfully converted into their corresponding oxathiolane, dithiolane, and dithiane derivatives with 2-mercaptoethanol, 1,2-ethanedithiol, and 1,3-propanedithiol using catalytic amount of yttrium triflate. In addition, by us

Synthesis of dibenzylbutyrolactone lignans: Total synthesis of arctigenin, pluviatolide and haplomyrfolin by tandem conjugate addition

Mitra, Jayati,Mitra, Alok Kumar

, p. 953 - 956 (2007/10/02)

The total synthesis of three dibenzylbutyrolactone lignans, arctigenin, pluviatolide and haplomyrfolin has been carried out by tandem cnjugate addition of dithiane carbanions to but-2-en-4-olide and substituted benzyl bromides leading to the formation of key intermediates which subsequently underwent debenzylation and desulphurisation.

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