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61490-17-3

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61490-17-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61490-17-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,4,9 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61490-17:
(7*6)+(6*1)+(5*4)+(4*9)+(3*0)+(2*1)+(1*7)=113
113 % 10 = 3
So 61490-17-3 is a valid CAS Registry Number.

61490-17-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Episamarcandin

1.2 Other means of identification

Product number -
Other names ferucrin

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:61490-17-3 SDS

61490-17-3Upstream product

61490-17-3Downstream Products

61490-17-3Relevant articles and documents

TERPENOID COUMARINS OF Ferula kokanica

Nabiev, A. A.,Khasanov, T. Kh.,Malikov, V. M.

, p. 547 - 549 (2007/10/02)

From an alcoholic extract of the roots of Ferula kokanica Rgl. et Schmalh., collected in the region of the village of Oman-kutan (Samarkand Province), have been isolated polyanthinin, mogoltadone, gummosin, kellerin, feshurin, and umbelliferone, and two new coumarins: deacetylkellerin, C24H32O5, M+ 400, mp 134-136 deg C, D22 +52 deg (c 0.1, ethanol), and kokanidin, C26H34O6, M+ 442, mp 189-191 deg C, D18 -30 deg (c 0.1, ethanol).The structure of deacetylkellerin has been established on the basis of the results of a study of UV, IR, PMR, and mass spectra.The structure and configuration of kokanidin have been established on the basis of spectral characteristics and also conversion into conferol acetate and feshurin.

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