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119318-15-9

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119318-15-9 Usage

General Description

Olean-12-ene-3,24-diol is a chemical compound found in plants, including various fruits and vegetables. It is classified as a triterpenoid, a group of naturally occurring organic chemicals derived from plants. Olean-12-ene-3,24-diol has been studied for its potential health benefits, including anti-inflammatory and antioxidant properties. It has also been examined for its potential anti-cancer and anti-diabetic effects. Research on this compound is ongoing, but initial findings suggest that it could have a range of therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 119318-15-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,3,1 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 119318-15:
(8*1)+(7*1)+(6*9)+(5*3)+(4*1)+(3*8)+(2*1)+(1*5)=119
119 % 10 = 9
So 119318-15-9 is a valid CAS Registry Number.

119318-15-9SDS

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 Olean-12-ene-3,24-diol

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:119318-15-9 SDS

119318-15-9Relevant articles and documents

TRITERPENOIDS FROM SYMPLOCOS RACEMOSA BARK

Ali, M.,Bhutani, K. K.,Srivastava, T. N.

, p. 3601 - 3604 (1990)

Three new triterpenes have been isolated from the stem bark of Symplocos racemosa together with the two known triterpenoids betulin and oleanolic acid.Their structures were characterized as 28-hydroxy-20α-urs-12,18(19)-dien-3β-yl acetate, 3-oxo-urs-20α-12,18(19)-dien-28-oic acid and 24-hydroxyolean-12-en-3-one by spectral and chemical means.

Triterpenes from the Leaves of Parsonsia Laevigata

Ogihara, Kazuhito,Higa, Matsutake,Hokama, Kozo,Suga, Takayuki

, p. 783 - 786 (1987)

A novel taraxerane-type triterpene-diol, in addition to taraxerol and lupeol, was isolated from the leaves of Parsonsia laevigata.Its structure was shown to be (4β)-D-friedoolean-14-ene-3β,24-diol (taraxer-14-ene-3β,24-diol) by a combination of chemical and spectroscopic methods.Key Word Index - Parsonsia laevigata; Apocynaceae; taraxerane-type triterpenoid; (4β)-D-friedoolean-14-ene-3β,24-diol.

Triterpenoid derivatives from Cylicodiscus gabunensis

Mkounga, Pierre,Tiabou, Alembert Tchinda,Kouam, Jacques

experimental part, p. 1100 - 1102 (2010/11/16)

Three new olean-12-ene derivatives (1-3), together with known urs-12-ene-3β, 28-diol (4) were isolated from the stem root of Cylicodiscus gabunensis. The structures of the new compounds were established by chemical and spectroscopic means as β-amyrin-n-no

Synthesis and hepatoprotective effects of soyasapogenol B derivatives

Sasaki, Kazue,Minowa, Nobuto,Kuzuhara, Hiroyuki,Nishiyama, Shoji,Omoto, Shoji

, p. 85 - 88 (2007/10/03)

Derivatives of soyasapogenol B (1), which is the aglycon moiety of soyasaponins from soybean, were synthesized and evaluated for their hepatoprotective effects in vitro.

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