Welcome to LookChem.com Sign In|Join Free

CAS

  • or

6973-62-2

Post Buying Request

6973-62-2 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

6973-62-2 Usage

Chemical Properties

Yellow Oil

Check Digit Verification of cas no

The CAS Registry Mumber 6973-62-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,7 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6973-62:
(6*6)+(5*9)+(4*7)+(3*3)+(2*6)+(1*2)=132
132 % 10 = 2
So 6973-62-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O5/c1-7(11)13-5-9-3-4-10(15-9)6-14-8(2)12/h9-10H,3-6H2,1-2H3

6973-62-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name [5-(acetyloxymethyl)oxolan-2-yl]methyl acetate

1.2 Other means of identification

Product number -
Other names 2,5-BISHYDROXYMETHYL TETRAHYDROFURAN DIACETATE

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:6973-62-2 SDS

6973-62-2Downstream Products

6973-62-2Relevant articles and documents

Chiral Pool/Henry/Enzymatic routes to acetogenin synthons

Qayed, Wesam S.,Luzzio, Frederick A.

, p. 622 - 630 (2015/11/09)

Enantio specific and enantioselective approaches to the natural (16 R,19R)- and the unnatural (16S,19S)- THF core of the bioactive acetogenin annonacin are described which utilizes both a chiral pool synthesis and enzymatic transformations. In the antipodal (2S,5S) THF series derived from D-(+)-glucosamine, the semi-protected THF aldehyde synthon allows for two-directional synthetic elaboration through a Henry reaction with a lipid-like nitroalkane. The resulting nitroalcohol having the unnatural (2S,5S)-THF core was oxidized to the corresponding a-nitroketone using a modified Collins oxidation. The intermediate a-nitroketone has potential for the preparation of the C15-C32 core and analogues through subsequent removal of the nitro group and reduction of the carbonyl.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 6973-62-2