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4871-87-8

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4871-87-8 Usage

Definition

ChEBI: A pentacyclic triterpenoid with formula C30H48O4, originally isolated from Akebia quinata and Stauntonia hexaphylla.

Check Digit Verification of cas no

The CAS Registry Mumber 4871-87-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,7 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4871-87:
(6*4)+(5*8)+(4*7)+(3*1)+(2*8)+(1*7)=118
118 % 10 = 8
So 4871-87-8 is a valid CAS Registry Number.
InChI:InChI=1/C30H48O4/c1-25(2)21-9-12-29(6)22(27(21,4)11-10-23(25)32)8-7-19-20-17-26(3,18-31)13-15-30(20,24(33)34)16-14-28(19,29)5/h7,20-23,31-32H,8-18H2,1-6H3,(H,33,34)/t20-,21?,22-,23+,26?,27+,28-,29-,30+/m1/s1

4871-87-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (4aR,6aR,6aS,6bR,10S,12aR,14bR)-10-hydroxy-2-(hydroxymethyl)-2,6a,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid

1.2 Other means of identification

Product number -
Other names Mesembryanthemoidigenic acid

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:4871-87-8 SDS

4871-87-8Upstream product

4871-87-8Downstream Products

4871-87-8Relevant articles and documents

Ebenamariosides A-D: Triterpene glucosides and megastigmanes from the leaves of diospyros maritima

Aramoto, Mitsunori,Inagaki, Masanori,Kawakami, Susumu,Matsunami, Katsuyoshi,Miura, Erika,Nishimura, Motohiro,Nobe, Ayaka,Otsuka, Hideaki

, p. 1337 - 1346 (2019/12/23)

The 1-BuOH-soluble fraction of the methanol (MeOH) extract of Diospyros maritima was separated by chromatographic techniques to give three new oleanane-type and one new ursane-type triterpene glucoside, named ebenamariosides A-D (1-4); two megastigmanes were also isolated. The structures of triterpene glucosides was elucidated with extensive investigation by one and two dimensional NMR spectroscopy and the structures were confirmed by partial enzymatic hydrolyses to give the corresponding mono-glucosides and aglycones. The structures of the megastigmanes, including their absolute stereochemistries, were elucidated by spectroscopic evidence and by the modified Mosher's method. Two megastigmanes were chemically correlated and their absolute structures were unambiguously determined. The cytotoxicity of the triterpene glucosides and their degradation products were assayed. They did not show any significant activity.

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