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14772-54-4

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  • (3S,9R,10S,13R,14S,17R)-3-HYDROXY-4,4,10,13-TETRAMETHYL-17-[(2R)-6-MET HYLHEPTAN-2-YL]-2,3,5,6,9,11,12,15,16,17-DECAHYDRO-1H-CYCLOPENTA[A]PHE NANTHRENE-14-CARBALDEHYDECAS

    Cas No: 14772-54-4

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14772-54-4 Usage

General Description

The chemical compound "(3S,9R,10S,13R,14S,17R)-3-hydroxy-4,4,10,13-tetramethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-14-carbaldehyde" is a complex organic compound with a long and specific molecular structure. It is composed of various functional groups including hydroxyl, methyl, and carbonyl groups. The compound is classified as a steroid derivative, and it possesses a cyclic structure with multiple carbon rings. The presence of the carbaldehyde group indicates potential reactivity and the ability to participate in chemical reactions. (3S,9R,10S,13R,14S,17R)-3-hydroxy-4,4,10,13-tetramethyl-17-[(2R)-6-met hylheptan-2-yl]-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phe nanthrene-14-carbaldehyde may have potential applications in the pharmaceutical or chemical industries, and further research may be needed to elucidate its properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 14772-54-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,7,7 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14772-54:
(7*1)+(6*4)+(5*7)+(4*7)+(3*2)+(2*5)+(1*4)=114
114 % 10 = 4
So 14772-54-4 is a valid CAS Registry Number.
InChI:InChI=1/C30H50O2/c1-20(2)9-8-10-21(3)22-14-18-30(19-31)24-11-12-25-27(4,5)26(32)15-16-28(25,6)23(24)13-17-29(22,30)7/h11,19-23,25-26,32H,8-10,12-18H2,1-7H3/t21-,22-,23+,25?,26+,28-,29-,30-/m1/s1

14772-54-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3β-Hydroxylanost-7-en-30-al

1.2 Other means of identification

Product number -
Other names 3β-hydroxy-lanost-7-en-30-al

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:14772-54-4 SDS

14772-54-4Upstream product

14772-54-4Downstream Products

14772-54-4Relevant articles and documents

Synthesis of 14-&α-Aminomethyl substituted Lanosterol Derivatives; Inhibitors of Fungal Ergosterol Biosynthesis

Cooper, Alan B.,Wright, John J.,Ganguly, Ashit K.,Desai, Jagdish,Loebenberg, David,et al.

, p. 898 - 900 (1989)

Several 14-α-aminomethyl-substituted lanosterol derivatives have been synthesized involving a complete Δ7,8 to Δ8,9 isomerization; these compounds are inhibitors of fungal ergosterol biosynthesis and are active against intact Candida and dermatophyte strains.

STEROIDAL 14ALPHA-CARBOXY-ALKYL DERIVATIVES AS REGULATORS OF HMG-COA REDUCTASE

-

, (2008/06/13)

New 14α-carboxyalkyl sterols are regulators of HMG-CoA reductase and inhibitors of mammalian 14α-methyl demethylase and are useful in lowering serum cholesterol levels and treating fungal infections.

The synthesis of some 32-functionalised lanostane derivatives.

Batten,Bentley,Boar,Draper,McGhie,Barton

, p. 739 - 748 (2007/10/04)

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