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15399-43-6

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15399-43-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15399-43-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,3,9 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 15399-43:
(7*1)+(6*5)+(5*3)+(4*9)+(3*9)+(2*4)+(1*3)=126
126 % 10 = 6
So 15399-43-6 is a valid CAS Registry Number.

15399-43-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (3R,4R,4aS,5S,6R,6aS,6bR,10S,12aR,14bS)-4a-Hydroxymethyl-2,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydro-picene-3,4,5,6,10-pentaol

1.2 Other means of identification

Product number -
Other names -

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:15399-43-6 SDS

15399-43-6Upstream product

15399-43-6Downstream Products

15399-43-6Relevant articles and documents

Medicinal flowers. XXXVI.1) Acylated oleanane-type triterpene saponins with inhibitory effects on melanogenesis from the flower buds of Chinese Camellia japonica

Nakamura, Seikou,Fujimoto, Katsuyoshi,Nakashima, Souichi,Matsumoto, Takahiro,Miura, Tomoko,Uno, Kaoru,Matsuda, Hisashi,Yoshikawa, Masayuki

experimental part, p. 752 - 758 (2012/09/25)

Four acylated oleanane-type triterpene oligoglycosides, sanchakasaponins E-H, were isolated from the flower buds of Camellia japonica cultivated in Yunnan province, China, together with four known triterpene oligoglycosides. The chemical structures of the new triterpene oligoglycosides were elucidated on the basis of chemical and physicochemical evidence. The inhibitory effects of the triterpene oligoglycoside constituents on melanogenesis in theophylline-stimulated B16 melanoma 4A5 cells were investigated.

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