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20881-03-2

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20881-03-2 Usage

General Description

1,2:3,4-Di-O-isopropylidene-beta-D-arabinopyranose is a chemical compound commonly used in the field of organic chemistry. It is a derivative of arabinose, a type of sugar, and is often utilized as a precursor in the synthesis of other compounds. This particular compound is characterized by its isopropylidene groups, which are functional groups that are commonly used to protect certain functional groups in organic synthesis. The compound is known for its stability and is commonly used in the protection and deprotection of various hydroxyl groups in organic synthesis. Additionally, it is used in the preparation of various pharmaceuticals and natural products due to its versatility and reactivity in organic reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 20881-03-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,8,8 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 20881-03:
(7*2)+(6*0)+(5*8)+(4*8)+(3*1)+(2*0)+(1*3)=92
92 % 10 = 2
So 20881-03-2 is a valid CAS Registry Number.

20881-03-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2:3,4-DI-O-ISOPROPYLIDENE-β-D-ARABINOPYRANOSE

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:20881-03-2 SDS

20881-03-2Downstream Products

20881-03-2Relevant articles and documents

Diastereoselective Michael-Claisen cyclizations of γ-oxa-α,β-unsaturated ketones en route to 5-oxatetracyclines

Liu, Fan,Wright, Peter M.,Myers, Andrew G.

, p. 206 - 209 (2017)

5-Oxatetracyclines were synthesized from D-arabinose using sequential Michael-Claisen cyclization reactions via a 5-oxa-AB enone substrate. The 5-oxatetracyclines were found to have poor stability in aqueous buffer (pH 7.4, 37°C) and showed little to no inhibition of bacterial growth (S. aureus, E. coli).

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