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[5α,8β,9α,10β,13β,16S,(+)]-Kaurane-16-ol is a naturally occurring kaurane-type diterpenoid, characterized by its unique stereochemistry and structure. This organic compound is derived from plants and is known for its various biological activities, such as anti-inflammatory, antitumor, and antimicrobial properties. It features a kaurane skeleton with a hydroxyl group at the C-16 position, and its stereochemistry is defined by the presence of specific chiral centers at the C-5, C-8, C-9, C-10, C-13, and C-16 positions. The compound's (+) configuration indicates that it is the enantiomer with a positive specific rotation. Due to its potential therapeutic applications, [5α,8β,9α,10β,13β,16S,(+)]-Kaurane-16-ol has been the subject of research in the field of natural product chemistry and pharmacology.

5524-17-4

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5524-17-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5524-17-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,2 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5524-17:
(6*5)+(5*5)+(4*2)+(3*4)+(2*1)+(1*7)=84
84 % 10 = 4
So 5524-17-4 is a valid CAS Registry Number.
InChI:InChI=1/C20H34O/c1-17(2)9-5-10-18(3)15(17)8-11-20-12-14(6-7-16(18)20)19(4,21)13-20/h14-16,21H,5-13H2,1-4H3

5524-17-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Kauran-16-ol

1.2 Other means of identification

Product number -
Other names (-)-16-hydroxy-dihydrokaurene

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:5524-17-4 SDS

5524-17-4Downstream Products

5524-17-4Relevant academic research and scientific papers

Structure of a novel diterpenoid ester, fritillahupehin from bulbs of Fritillaria hupehensis Hsiao and K.C. Hsia

Ruan, Hanli,Zhang, Yonghui,Wu, Jizhou,Deng, Shukai,Sun, Handong,Fujita, Tetsuro

, p. 288 - 291 (2007/10/03)

A new diterpenoid ester, fritillahupehin (1) together with three known fatty acids: palmitic acid (2), lignoceric acid (3) and azelaic acid (4) were isolated from the bulbs of Fritillaria hupehensis Hsiao and K.C. Hsia. The structure of fritillahupehin has been established to be ent-kauran-16β-yl lignocerate by means of spectroscopic and chemical evidence. Compounds 2-4 were isolated from Fritillaria sp. for the first time.

TERPENOIDS OF THE LIVERWORT FRULLANOIDES DENSIFOLIA AND TROCHOLEJEUNEA SANDVICENSIS

Tori, Motoo,Arbiyanti, Hernita,Taira, Zenei,Asakawa, Yoshinori

, p. 335 - 348 (2007/10/02)

Two new rearranged pinguisane-type sesquiterpenoids, spirodensifolin A and B, a pinguisane-type sesquiterpene, isonaviculol, and two new ent-kaurane-type diterpenoids, ent-kauran-16β-ol-3-one, ent-kaurane-3β,16β-diol, have been isolated from the Bolivian liverwort Frullanoides densifolia, and a pinguisane-type sesquiterpene, furanopinguisanol and lepidozane-type sesquiterpene alcohol have been isolated from the Japanese Trocholejeunea sandvicensis.Their stereostructures have been elucidated by the extensive analysis of the spectral data as well as the X-ray crystallographic analysis.Key Word Index - Frullanoides densifolia; Trocholejeunea sandvicensis; Lejeuneaceae; liverwort; Hepaticae; chemosystematics; spirodensifolin A; spirodensifolin B; furanopinguisanol; pinguisane-type sesquiterpenoids; ent-kauranols; kaurane-type diterpenoids; lepidozenol; lepidozane-type sesquiterpenoid.

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