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3327-63-7

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3327-63-7 Usage

General Description

Ribonolactone, also known as ribose lactone, is a chemical compound with the molecular formula C5H8O4. It is a cyclic ester of ribonic acid, which is a derivative of ribose. Ribonolactone has been studied for its potential pharmaceutical and medicinal properties, including its antioxidant and anti-inflammatory effects. It is also a precursor to various biologically important compounds, such as riboflavin and nucleotides. Additionally, ribonolactone has been investigated for its potential as a biomarker for certain diseases and metabolic pathways. Its unique structure and potential biological activities make it a subject of interest for researchers in the fields of biochemistry, pharmaceuticals, and medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 3327-63-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,2 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3327-63:
(6*3)+(5*3)+(4*2)+(3*7)+(2*6)+(1*3)=77
77 % 10 = 7
So 3327-63-7 is a valid CAS Registry Number.

3327-63-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ribonolactone

1.2 Other means of identification

Product number -
Other names DL-arabinonic acid-4-lactone

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:3327-63-7 SDS

3327-63-7Relevant articles and documents

A new efficient access to glycono-1,4-lactones by oxidation of unprotected itols by catalytic hydrogen transfer with RhH(PPh3)4-benzalacetone system

Isaac,Aizel,Stasik,Wadouachi,Beaupère

, p. 475 - 476 (2007/10/03)

Treatment of unprotected pentitols and hexitols with RhH(PPh3)4-benzalacetone system leads exclusively to glycono-1,4-lactones in 60-96% yield.

Stereoselective Samarium(II)-induced Coupling of β-Silylacrylic Esters: a Synthesis of (+/-)-2-Deoxyribonolactone

Fleming, Ian,Ghosh, Sunil K.

, p. 1775 - 1777 (2007/10/02)

Samarium iodide converts the β-silylacrylate 1c with high stereoselectivity into the racemic diester 2c, from which (+/-)deoxyribonolactone 11 can be prepared.

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