19043-54-0

• 

• Basic information

  1. Product Name: 5-hydroxycholestan-6-one
  2. Synonyms:
  3. CAS NO:19043-54-0
  4. Molecular Formula: C₂₇H₄₆O₂
  5. Molecular Weight: 402.6529
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 19043-54-0.mol
  9. Article Data: 4

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 496.7°C at 760 mmHg
  3. Flash Point: 210.6°C
  4. Appearance: N/A
  5. Density: 1.013g/cm³
  6. Vapor Pressure: 6.02E-12mmHg at 25°C
  7. Refractive Index: 1.517
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 5-hydroxycholestan-6-one(CAS DataBase Reference)
  11. NIST Chemistry Reference: 5-hydroxycholestan-6-one(19043-54-0)
  12. EPA Substance Registry System: 5-hydroxycholestan-6-one(19043-54-0)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 19043-54-0(Hazardous Substances Data)

• Suppliers
• Usage
• SDS
• Upstream product
• Downstream Products
• Article

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• 5-hydroxy-10,13-dimethyl-17-(6-methylheptan-2-yl)-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-6-one

  Cas No: 19043-54-0

• USD $ 3.0-3.0 / Kilogram

• 1 Kilogram

• 1-100 Metric Ton/Month

• Dayang Chem (Hangzhou) Co.,Ltd.
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• 5-hydroxy-10,13-dimethyl-17-(6-methylheptan-2-yl)-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-6-one cas 19043-54-0

  Cas No: 19043-54-0

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19043-54-0 Usage

Classification

Ketone derived from cholesterol

Origin

Natural metabolite found in the human body

Biological Significance

Potential marker for metabolic disorders and diseases

Research Focus

Cholesterol Metabolism: Studied for its roles in cholesterol metabolism
Biomarker: Investigated as a biomarker for liver and gallbladder diseases
Therapeutic Potential: Explored for therapeutic applications, including:
Inhibition of 17β-hydroxysteroid dehydrogenase type 10 activity

Medical and Biochemical Relevance

Compound of interest for diagnostic and therapeutic purposes in medicine and biochemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 19043-54-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,4 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19043-54:
(7*1)+(6*9)+(5*0)+(4*4)+(3*3)+(2*5)+(1*4)=100
100 % 10 = 0
So 19043-54-0 is a valid CAS Registry Number.

19043-54-0SDS

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	5-hydroxy-10,13-dimethyl-17-(6-methylheptan-2-yl)-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-6-one

1.2 Other means of identification

Product number	-
Other names	5-Hydroxycholestan-6-one

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:19043-54-0 SDS

19043-54-0Upstream product

• 1912-53-4 6-nitrocholest-5-ene 
• 20230-22-2 5,6β-epoxy-5β-cholestane 
• 66014-22-0 6β-Chloro-5-hydroxy-5α-cholestane 
• 333-20-0 potassium thioacyanate 
• 75-77-4 chloro-trimethyl-silane 

19043-54-0Downstream Products

• 481-21-0 cholestane 
• 570-46-7 5α-cholestan-6-one 

19043-54-0Relevant articles and documents

Microwave-assisted transformation of α,β- and β,γ-unsaturated nitroalkenes into carbonyl compounds

Das, Deba D.,Nayak, Amalendu,Nanda, Bhagabat,Das, Nalin B.

, p. 481 - 482 (2007/10/03)

Vinyl and allylic nitroalkenes have been converted into the corresponding carbonyl compounds in good yield using tin(II) chloride dihydrate under microwave irradiation.

Synthesis of Cholestenothiazoles and Cholestanooxazolidine

Ahmad, M. S.,Alam, Zafar

, p. 486 - 488 (2007/10/02)

4β,5-Epoxy-5β-cholestan-3-one (I) reacts with thiourea to afford 5β-hydroxycholest-3-eno-2'-aminothiazole (II) while with thiacetamide it furnishes 3,5-cholestadieno-2'-methylthiazole (III) and 5β-hydroxycholest-3-eno-2'-methylthiazole (IV). 6β-Chloro-5-hydroxy-5α-cholestane (V) on treatment with KSCN in dimethylformamide gives cholesta-4,6-diene (VI), 5α-chloestan-6-one (VII), 5-hydroxy-5α-cholestan-6α-yl isothiocyanate (VIII), 5-hydroxy-5α-cholestan-6-one (IX) and 5α-cholestano-2'-thiooxooxazolidine (X).The structures of these compounds have been established on the basis of spectral properties, analytical data and also by direct comparison with authentic samples where available.

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