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86408-17-5

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86408-17-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86408-17-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,4,0 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 86408-17:
(7*8)+(6*6)+(5*4)+(4*0)+(3*8)+(2*1)+(1*7)=145
145 % 10 = 5
So 86408-17-5 is a valid CAS Registry Number.

86408-17-5SDS

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 ASKENDOSIDE D

1.2 Other means of identification

Product number -
Other names N-[ETHYL-(2-METHOXYPHENYL)ARSANYL]-N-METHYL-METHANAMINE

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:86408-17-5 SDS

86408-17-5Upstream product

86408-17-5Relevant articles and documents

TRITERPENE GLYCOSIDES OF Astragalus AND THEIR GENINS. XII. ASKENDOSIDE B FROM Astragalus taschkendicus

Isaev, M. I.,Gorovits, M. B.,Abdullaev, N. D.,Abubakirov, N. K.

, p. 428 - 431 (1983)

On the basis of chemical transformations and with the aid of physicochemical characteristics it has been established that a new glycoside of the cycloartane series - askendoside B (I) - isolated from the roots of Astragalus taschkendicus Bge., is 20S,24R-epoxycycloartane-3β,6α,16β,25-tetraol 3-O-2)-(3'-O-acetyl-β-D-xylopyranoside)> 6-O-β-D-xylopyranoside, C47H76O18, mp 215-218 deg C, 20D -45.5 deg (c 1.1; pyridine).The acid hydrolysis of (I) yielded cyclosiversigenin (II) with mp 239-241 deg C, 20D +54.5 deg (c 1.2; MeOH), and cyclosiversigenin 3-O-β-D-xylopyranoside (III) with mp 262-264 deg C, 20D +41 deg (c 0.4; MeOH).The periodate oxidation of glycoside (I) followed by acid hydrolysis likewise led to (II) and to D-xylose.The alkaline hydrolysis of (I) yielded askendoside D (IV), with mp 235-236 deg C, 23D -8.5 deg (c 1.0; pyridine).The Smith degradation of (I) led to (III).The IR and PMR spectra of (I) are given.

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