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2309-45-7

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2309-45-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2309-45-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,0 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2309-45:
(6*2)+(5*3)+(4*0)+(3*9)+(2*4)+(1*5)=67
67 % 10 = 7
So 2309-45-7 is a valid CAS Registry Number.

2309-45-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3β,16α-dihydroxy-olean-12-en-28-oic acid methyl ester

1.2 Other means of identification

Product number -
Other names 3β,16α-Dihydroxy-olean-12-en-28-saeure-methylester

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:2309-45-7 SDS

2309-45-7Relevant articles and documents

Kubota et al.

, p. 771 (1969)

An echinocystic acid saponin derivative from Kalimeris shimadae

Shao, Yu,Poobrasert, Onoomar,Ho, Chi-Tang,Chin, Chee-Kok,Cordell, Geoffrey A.

, p. 195 - 200 (2007/10/03)

A new triterpene saponin, shimadoside A, has been isolated from Kalimeris shimadae and its structure deduced as 3-O-β-D- glucopyranosiduronic acid-3β-16α-dihydroxyolean-12-en-28-oic acid 28-O-β- D-xylopyranosyl-(1 → 3)-β-D-xylopyranosyl (1 → 4)-α-L-rhamnopyranosyl-(1 → 2)-β-D-xylopyranoside by means of spectral data, especially NMR, including COSY, HMQC, HOHAHA and ROESY techniques, and chemical degradation.

Study of Saponins from Albizzis lebbek Benth Flowers

Varshney, I. P.,Jain, D. C.,Srivastava, H. C.

, p. 884 - 887 (2007/10/02)

Albizzia lebbek Benth flowers yield a number of saponins named as lebbekanin-D, F, G, and H.They are all glycosides of echinocystic acid with varying sugars.On the basis of enzymatic, partial alkaline hydrolysis, methylation and periodate oxidation studies, partial structures have been assigned to these saponins.

STRUCTURES OF 3,28-O-BISGLYCOSIDIC TRITERPENOID SAPONINS OF FATSIA JAPONICA

Akoi, Tadashi,Shido, Kazumi,Takahashi, Yutaka,Suga, Takayuki

, p. 1681 - 1686 (2007/10/02)

Four novel 3,28-O-bisglycosidic triterpenoid saponins were isolated from the mature fruits of F. japonica.They were characterized as the 28-O-α-L-rhamnopyranosyl-(1->4)-β-D-glucopyranosyl-(1->4)-β-D-glucopyranosides of 3-O-α-L-arabinopyranosyl echinocystic acid, 3-O-α-L-arabinopyranosyl hederagenin, 3-O-β-D-glucopyranosyl-(1->2)-α-L-arabinopyranosyl oleanolic acid and 3-O-β-D-glucopyranosyl-(1->2)-α-L-arabinopyranosyl hederagenin respectively. - Keywords: Fatsia japonica; Araliaceae; mature fruits; 3,28-O-bisglycidic triterpenoid saponins.

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