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(20S)-3β,20-Dihydroxylanosta-7,9(11)-diene-18-oic acid γ-lactone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24041-68-7

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24041-68-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24041-68-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,4 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 24041-68:
(7*2)+(6*4)+(5*0)+(4*4)+(3*1)+(2*6)+(1*8)=77
77 % 10 = 7
So 24041-68-7 is a valid CAS Registry Number.

24041-68-7SDS

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 seychellogenin

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:24041-68-7 SDS

24041-68-7Downstream Products

24041-68-7Relevant academic research and scientific papers

Marine Natural Products. XVIII. Four Lanostane-Type Triterpene Oligoglycosides, Bivittosides A, B, C, and D, from the Okinawan Sea Cucumber Bohadschia bivittata MITSUKURI

Kitagawa, Isao,Kobayashi, Motomasa,Hori, Manabu,Kyogoku, Yoshimasa

, p. 61 - 67 (2007/10/02)

A full account of the structure elucidation of four lanostane-type triterpene oligoglycosides, bivittosides A (6), B (8), C (9), and D (10), is presented.Bivittosides were isolated from body-walls and Cuvierian tubules of the Okinawan sea cucumber Bohadschia bivittata MITSUKURI, and among these four oligoglycosides, bivittoside D (10) showed significant antifungal activities.Acidic hydrolysis of bivittosides A (6), B (8), and D (10) provided three artifact sapogenols, among which a homoannular-dienic sapogenol named preseychellogenin (4), exhibiting characteristically red-shifted ultraviolet and circular dichroism spectra, was identified as the monoacetate (4a).Keywords: sea cucumber; Bohadschia bivittata; bivittoside; lanostane-type triterpene oligoglycoside; homoannular-diene strained; oligoglycoside 13C-NMR; oligoglycoside T1; Turbo cornutus glycosidase; deoxybivittogenin; preseychellogenin

MARINE NATURAL PRODUCTS. XIX. PERVICOSIDES A, B, AND C, LANOSTANE-TYPE TRITERPENE-OLIGOGLYCOSIDE SULFATES FROM THE SEA CUCUMBER HOLOTHURIA PERVICAX

Kitagawa, Isao,Kobayashi, Motomasa,Son, Byeng Wha,Suzuki, Shigeki,Kyogoku, Yoshimasa

, p. 1230 - 1234 (2007/10/02)

Triterpene-oligoglycoside constituents, contained in the body walls and the Cuvierian tubules of the sea cucumber Holothuria pervicax (torafu-namako in Japanese), were investigated and purified in their desulfated forms.These desulfated lanostane-type triterpene tetraglycosides, designated DS-pervicoside A (7), DS-pervicoside B (8), and DS-pervicoside C (9), have antifungal activity, and their structures were determined on the basis of chemical and physicochemical evidence.The parent oligoglycosides of these desulfated tetraglycosides, named pervicosides A (10), B (11), and C (12), were shown to be the 4'-sulfates of DS-pervicosides A (7), B (8), and C (9), respectively.Keywords: sea cucumber; Holothuria pervicax; oligoglycoside antifungal; lanostane-type triterpene oligoglycoside; oligoglycoside 13C-NMR; pervicoside A; pervicoside B; pervicoside C

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