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132970-47-9

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132970-47-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132970-47-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,9,7 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 132970-47:
(8*1)+(7*3)+(6*2)+(5*9)+(4*7)+(3*0)+(2*4)+(1*7)=129
129 % 10 = 9
So 132970-47-9 is a valid CAS Registry Number.

132970-47-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name ((3R,5S)-5-Hydroxymethyl-2-oxo-tetrahydro-furan-3-yl)-carbamic acid benzyl ester

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:132970-47-9 SDS

132970-47-9Downstream Products

132970-47-9Relevant articles and documents

A facile transformation of the δ-hydroxy-α-amino lactones from α- furfuryl amide

Liao, Li-Xin,Zhou, Wei-Shan

, p. 12571 - 12584 (2007/10/03)

(S)- and (R)- α- furfuryl amides, obtained from the kinetic resolution of (R, S)- α- furfuryl amide using the modified Sharpless asymmetric epoxidation, have been transformed into four 8-hydroxy α- amino lactones (1S, 3S)-1, (1R, 3R)-1, (1S, 3R)-1, (1R, 3S)-1, using sharpless asymmetric dihydroxylation as the key step. The much more efficient method of the addition of chiral aldimine 10 with allylic Grignard reagent for preparation of (S, S)-1 was also achieved.

Amino acids and peptides; 75. Synthesis of di- and trihydroxyamino acids - Construction of lipophilic tripalmitoyldihydroxy-α-amino acids

Schmidt,Lieberknecht,Kazmaier,Griesser,Jung,Metzger

, p. 49 - 55 (2007/10/02)

Suitable protected derivatives of trihydroxynorleucines-[(2S,4S,5S)- and (2R,4S,5S)-2-amino-4,5,6-trihydroxyhexanoic acid], of all isomeric dihydroxynorvalines [2-amino-4,5-dihydroxypentanoic acids), of all isomeric 2-amino-6,7-dihydroxyheptanoic acids an

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