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2-phenyl-2-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxa n-2-yl]oxymethyl]oxan-2-yl]oxy-acetonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51371-34-7

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51371-34-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51371-34-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,3,7 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 51371-34:
(7*5)+(6*1)+(5*3)+(4*7)+(3*1)+(2*3)+(1*4)=97
97 % 10 = 7
So 51371-34-7 is a valid CAS Registry Number.
InChI:InChI=1/C20H27NO11/c21-6-10(9-4-2-1-3-5-9)30-20-18(28)16(26)14(24)12(32-20)8-29-19-17(27)15(25)13(23)11(7-22)31-19/h1-5,10-20,22-28H,7-8H2/t10?,11?,12?,13-,14-,15?,16?,17?,18?,19-,20-/m1/s1

51371-34-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzeneacetonitrile, .α.-[(6-O-.β.-D-glucopyranosyl-.β.-D-gluco-pyranosyl)oxy]-

1.2 Other means of identification

Product number -
Other names Isoamygdalin

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:51371-34-7 SDS

51371-34-7Upstream product

51371-34-7Relevant academic research and scientific papers

Study on the Prevention of Racemization of Amygdalin

Takayama, Yuzi,Kawai, Satoshi

, p. 778 - 781 (2007/10/02)

Studies were conducted to find suitable conditions for the prevention of racemization of amygdalin in aqueous solution.Evaluation of racemization was carried out by determination of the ratios of neoamygdalyn and amygdalin using a capillary gas chromatographic technique.Racemization of amygdalin in aqueous solution was accelerated by increases on pH and temperature, but racemization was low below pH 3.0 even with heating.Ascorbic acid is useful as an acidification reagent for the suppression of racemization, and has the added clinical benefit of vitamin C activity.Keywords - amygdalin; isoamygdalin separation; racemization; racemizati on prevention; capillary gas chromatography

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