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1'H-5α-Cholestano[3,2-b]indole is a complex organic compound with a molecular formula of C27H38N2. It is a derivative of cholestanol, a naturally occurring steroid, and indole, a heterocyclic aromatic organic compound. 1'H-5α-Cholestano[3,2-b]indole features a cholestane ring system fused to an indole ring, with the indole nitrogen atom positioned at the 5α position relative to the cholestane ring. The structure is characterized by the presence of a hydrogen atom at the 1' position, which is part of the indole ring. 1'H-5α-Cholestano[3,2-b]indole is of interest in chemical research due to its unique structure and potential applications in the development of new pharmaceuticals or other chemical products. However, it is important to note that the specific properties, reactivity, and applications of 1'H-5α-Cholestano[3,2-b]indole would require further investigation and study.

4356-25-6

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4356-25-6 Usage

Molecular Structure

A complex structure consisting of a cholestane backbone fused to an indole ring.

Compound Type

An uncommon steroid derivative.

Potential Activities

Pharmacological and biological activities, though limited research has been conducted.

Biological Effects of Cholestane Derivatives

Anti-inflammatory, antitumor, and neuroprotective properties.

Uniqueness

The fusion of cholestane and indole structures may result in unique biological activities.

Research Interest

An interesting target for further exploration in drug development and medical research.

Check Digit Verification of cas no

The CAS Registry Mumber 4356-25-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,5 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4356-25:
(6*4)+(5*3)+(4*5)+(3*6)+(2*2)+(1*5)=86
86 % 10 = 6
So 4356-25-6 is a valid CAS Registry Number.
InChI:InChI=1/C33H49N/c1-21(2)9-8-10-22(3)27-15-16-28-25-14-13-23-19-31-26(24-11-6-7-12-30(24)34-31)20-33(23,5)29(25)17-18-32(27,28)4/h6-7,11-12,21-23,25,27-29,34H,8-10,13-20H2,1-5H3/t22-,23+,25+,27-,28+,29+,32-,33+/m1/s1

4356-25-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (1r,3as,3br,5as,12as,12bs,14ar)-12a,14a-dimethyl-1-[(2r)-6-methylheptan-2-yl]-1,2,3,3a,3b,4,5,5a,6,7,12,12a,12b,13,14,14a-hexadecahydrocyclopenta[5,6]naphtho[2,1-b]carbazole

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:4356-25-6 SDS

4356-25-6Downstream Products

4356-25-6Relevant academic research and scientific papers

Cholesteno-Indoles, I. Preparation of 1'H-5α-Cholest-2-enoindoles

Samu, Janos,Botyanszki, Janos,Duddeck, Helmut,Snatzke, Guenther

, p. 1225 - 1228 (2007/10/02)

1'H-5α-Cholest-2-enoindole (1a), the corresponding N-methyl, N-acetyl, and N-formyl compounds 1b-d, as well as the respective methoxy derivatives 2b-5d have been synthesized as model compounds for intended CD investigations.Application of the Fischer indole synthesis afforded the compounds 1a-5a which were N-methylated to 1b-5b, N-acetylated to 1c-5c, and N-formylated to 1d-5d. - Key Words: Fischer indole synthesis / Cholestenoindoles / Cholestenes / Steroids

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