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4152-81-2

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4152-81-2 Usage

General Description

1,2-di-O-acetyl-3-O-benzoyl-5-deoxypentofuranose is a chemical compound with a complex structure containing acetyl and benzoyl functional groups attached to a pentofuranose ring. The compound is a deoxy sugar, meaning it is a sugar molecule with one or more hydroxyl groups replaced by hydrogen atoms. This particular deoxy sugar has additional acetyl and benzoyl groups attached to the hydroxyl groups on the sugar ring, contributing to its high level of complexity. These chemical properties make 1,2-di-O-acetyl-3-O-benzoyl-5-deoxypentofuranose suitable for use in various research and industrial applications, particularly in the field of organic chemistry and the synthesis of complex molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 4152-81-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,5 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4152-81:
(6*4)+(5*1)+(4*5)+(3*2)+(2*8)+(1*1)=72
72 % 10 = 2
So 4152-81-2 is a valid CAS Registry Number.

4152-81-2SDS

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 Catechol Dipropyl Ether

1.2 Other means of identification

Product number -
Other names 1,2-dipropoxy-benzene

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:4152-81-2 SDS

4152-81-2Downstream Products

4152-81-2Relevant articles and documents

First total synthesis of a naturally occurring iodinated 5′-deoxyxylofuranosyl marine nucleoside

Sun, Jianyun,Dou, Yanhui,Ding, Haixin,Yang, Ruchun,Sun, Qi,Xiao, Qiang

, p. 881 - 889 (2012/07/14)

4-Amino-7-(5′-deoxy-β-D-xylofuranosyl)-5-iodo-pyrrolo[2,3-d] pyrimidine 1, an unusual naturally occurring marine nucleoside isolated from an ascidan, Diplosoma sp., was synthesized from D-xylose in seven steps with 28% overall yield on 10 g scale. The key step was Vorbrueggen glycosylation of 5-iodo-pyrrolo[2,3-d]pyrimidine with 5-deoxy-1, 2-O-diacetyl-3-O-benzoyl-D- xylofuranose. Its absolute configuration was confirmed.

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