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7695-70-7

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7695-70-7 Usage

Chemical Properties

White Solid

Uses

Different sources of media describe the Uses of 7695-70-7 differently. You can refer to the following data:
1. Salicylic Acid β-D-O-Glucuronide is a metabolite of Acetylsalicylic Acid (Aspirin) (A187780).
2. A metabolite of Aspirin

Definition

ChEBI: A beta-D-glucosiduronic acid that is the glucuronide conjugate of salicyclic acid.

Check Digit Verification of cas no

The CAS Registry Mumber 7695-70-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,9 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7695-70:
(6*7)+(5*6)+(4*9)+(3*5)+(2*7)+(1*0)=137
137 % 10 = 7
So 7695-70-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H14O9/c14-7-8(15)10(12(19)20)22-13(9(7)16)21-6-4-2-1-3-5(6)11(17)18/h1-4,7-10,13-16H,(H,17,18)(H,19,20)/t7?,8-,9?,10?,13+/m0/s1

7695-70-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3S,4S,5R,6S)-6-(2-carboxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names Salicylic acid phenol glucuronide

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:7695-70-7 SDS

7695-70-7Downstream Products

7695-70-7Relevant articles and documents

Electroorganic synthesis 66: Selective anodic oxidation of carbohydrates mediated by TEMPO

Schnatbaum, Karsten,Sch?fer, Hans J.

, p. 864 - 872 (2007/10/03)

The carbohydrates 4-15 are anodically oxidized with 2,2,6,6- tetramethylpiperidin-1-oxyl (TEMPO) as mediator. Selective and complete reaction at the primary hydroxyl groups affords the corresponding carboxylic acids 16-32 in moderate to excellent yield. Methyl α-D-glucopyranoside is converted in 98% yield to the uronic acid 16. Cyclic voltammetry shows that the oxydation is base-catalyzed and the oxidation of the hydroxy group with TEMPO+ (2) is rate determining.

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