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50921-28-3

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50921-28-3 Usage

Functional groups

Benzyloxy, Sulfinyl, Alcohol

Chirality

Chiral sulfoxide compound

Synthesis

Reaction of 4-methylbenzenethiol with 3-chloropropionaldehyde, followed by condensation with benzyloxyamine

Applications

Intermediate in the synthesis of pharmaceuticals and other organic compounds

Industries

Pharmaceutical and agrochemical industries

Reactivity

Versatile reactivity

Stereochemistry

Unique stereochemistry

Check Digit Verification of cas no

The CAS Registry Mumber 50921-28-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,9,2 and 1 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 50921-28:
(7*5)+(6*0)+(5*9)+(4*2)+(3*1)+(2*2)+(1*8)=103
103 % 10 = 3
So 50921-28-3 is a valid CAS Registry Number.

50921-28-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-methylphenyl)sulfinyl-3-phenylmethoxypropan-2-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:50921-28-3 SDS

50921-28-3Downstream Products

50921-28-3Relevant articles and documents

A visible-light-induced thiol addition/aerobic oxidation cascade reaction of epoxides and thiols for the synthesis of β-hydroxylsulfoxides

Mamat, Marhaba,Liu, Changhong,Abdukerem, Dilshat,Abdukader, Ablimit

supporting information, p. 9855 - 9859 (2021/12/07)

A photochemical thiol addition/aerobic oxidation cascade reaction has been developed. This protocol enables efficient oxidative coupling of epoxides and thiols to access structurally valuable β-hydroxylsulfoxides. A broad range of functional groups are co

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