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"20-(2-carbamoylhydrazinylidene)pregn-5-en-3-yl acetate" is a complex organic compound with the molecular formula C25H36N2O3. It is a derivative of pregnane, a steroid with a cyclopentane ring fused to a hydrocarbon structure. The compound features a carbamoylhydrazinylidene group at the 20-position, which is a key structural element. This molecule is known for its potential applications in pharmaceuticals, particularly in the development of drugs targeting the glucocorticoid receptor, which plays a role in various physiological processes. The acetate group at the 3-position further modifies its chemical properties and potential interactions within biological systems.

6192-83-2

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6192-83-2 Usage

Properties

1. Chemical Name: 20-(2-carbamoylhydrazinylidene)pregn-5-en-3-yl acetate
2. Chemical Formula: C24H33N3O4
3. Molecular Weight: Approximately 419.54 g/mol
4. Class: Steroids and steroid derivatives
5. Derived from: Pregnenolone
6. Biological Activity: Potential due to the presence of the carbamoylhydrazine group
7. Physiological Effects: Requires further research for comprehensive understanding
8. Functional Groups: Carbamoylhydrazine and acetate groups

Specific Content

1. Pregn-5-en-3-yl Backbone: Derived from pregnenolone, a precursor hormone in the synthesis of various important hormones.
2. Carbamoylhydrazinylidene Group (NHCONHN=): Imparts potential biological activity, suggesting pharmacological relevance.
3. Acetate Group (COCH3): Indicates potential use as a chemical intermediate in organic synthesis.
4. Steroid Structure: Characteristic fused ring system with 4 rings (3 cyclohexane rings and 1 cyclopentane ring).
5. Hormonal Significance: As a derivative of pregnenolone, it may play a role in hormonal pathways, including cortisol, estrogen, and testosterone synthesis.
6. Complex Molecular Structure: Reflects the intricate arrangement of atoms and bonds, suggesting diverse potential applications and interactions in biological systems.
7. Potential Therapeutic Applications: Requires exploration due to its structural resemblance to steroid hormones, which are involved in various physiological processes.
8. Chemical Reactivity: Affected by the presence of functional groups, influencing its behavior in chemical reactions and interactions with other molecules.
9. Synthetic Accessibility: Feasibility of synthesis from pregnenolone and appropriate reagents, potentially enabling production for research and industrial purposes.

20-(2-carbamoylhydrazinylidene)pregn-5-en-3-yl acetate represents an intriguing intersection of organic chemistry, biochemistry, and pharmacology, with implications for both basic science and applied research.

Check Digit Verification of cas no

The CAS Registry Mumber 6192-83-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,9 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6192-83:
(6*6)+(5*1)+(4*9)+(3*2)+(2*8)+(1*3)=102
102 % 10 = 2
So 6192-83-2 is a valid CAS Registry Number.

6192-83-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Pregn-5-en-20-one, 3-(acetyloxy)-, 2-(aminocarbonyl)hydrazone, (3.β.)-

1.2 Other means of identification

Product number -
Other names oxime of pregnenolone acetate

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:6192-83-2 SDS

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