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60434-71-1

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60434-71-1 Usage

Chemical Properties

white crystals

Check Digit Verification of cas no

The CAS Registry Mumber 60434-71-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,4,3 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 60434-71:
(7*6)+(6*0)+(5*4)+(4*3)+(3*4)+(2*7)+(1*1)=101
101 % 10 = 1
So 60434-71-1 is a valid CAS Registry Number.
InChI:InChI=1/C17H20O6S2/c1-13-4-8-16(9-5-13)24(18,19)22-12-15(3)23-25(20,21)17-10-6-14(2)7-11-17/h4-11,15H,12H2,1-3H3/t15-/m0/s1

60434-71-1 Well-known Company Product Price

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  • Aldrich

  • (309656)  (S)-(−)-1,2-Propanedioldi-p-tosylate  99%

  • 60434-71-1

  • 309656-5G

  • 3,114.54CNY

  • Detail

60434-71-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-(-)-1,2-Propanediol di-p-tosylate

1.2 Other means of identification

Product number -
Other names 2-(4-methylphenyl)sulfonyloxypropyl 4-methylbenzenesulfonate

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:60434-71-1 SDS

60434-71-1Downstream Products

60434-71-1Relevant articles and documents

Synthesis of C2-symmetric chiral amino alcohols: Their usage as organocatalysts for enantioselective opening of epoxide ring

Turgut, Yilmaz,Aral, Tarik,Karakaplan, Mehmet,Deniz, Pinar,Hosgoren, Halil

experimental part, p. 3365 - 3377 (2011/01/04)

A series of -amino alcohols derivatives were synthesized from (R)-2-amino-1-butanol and (S)-1,2-propanediol, and they have been used as organocatalaysts in the racemic ring opening of epoxide in good yields with high enantiomeric excess (up to 97%). Copyright

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