1255-26-1

• 

• Basic information

  1. Product Name: lanost-8-en-3-one
  2. Synonyms:
  3. CAS NO:1255-26-1
  4. Molecular Formula: C₃₀H₅₀O
  5. Molecular Weight: 426.7174
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 1255-26-1.mol
  9. Article Data: 3

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 494.5°C at 760 mmHg
  3. Flash Point: 204.8°C
  4. Appearance: N/A
  5. Density: 0.97g/cm³
  6. Vapor Pressure: 6.39E-10mmHg at 25°C
  7. Refractive Index: 1.515
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: lanost-8-en-3-one(CAS DataBase Reference)
  11. NIST Chemistry Reference: lanost-8-en-3-one(1255-26-1)
  12. EPA Substance Registry System: lanost-8-en-3-one(1255-26-1)

• 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: 1255-26-1(Hazardous Substances Data)

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

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• Lanost-8-en-3-one

  Cas No: 1255-26-1

• USD $ 3.0-3.0 / Kilogram

• 1 Kilogram

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• Lanost-8-en-3-one cas 1255-26-1

  Cas No: 1255-26-1

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1255-26-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1255-26-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,5 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1255-26:
(6*1)+(5*2)+(4*5)+(3*5)+(2*2)+(1*6)=61
61 % 10 = 1
So 1255-26-1 is a valid CAS Registry Number.

1255-26-1SDS

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	4,4,10,13,14-pentamethyl-17-(6-methylheptan-2-yl)-1,2,5,6,7,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one

1.2 Other means of identification

Product number	-
Other names	Lanost-8-en-3-on

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:1255-26-1 SDS

1255-26-1Upstream product

• 79-62-9 24,25-dihydrolanosterol 
• 64-19-7 acetic acid 
• 59684-64-9 (5α)-tirucall-8-en-3β-ol 
• 79-63-0 tirucallol 
• 2671-68-3 lanosterol 
• 887608-61-9 lanosterol 
• 6593-55-1 lanosta-8,24-dien-3α-ol 

1255-26-1Downstream Products

• 79-62-9 24,25-dihydrolanosterol 
• 6593-55-1 lanosta-8,24-dien-3α-ol 
• 6593-21-1 lanost-8-ene 
• 118653-49-9 8α,9α-epoxy-5α-lanostan-3-one 
• 55401-48-4 5α-lanost-8-en-3,7-dione 
• 1575700-26-3 (5R,10S,13R,14R,17R,E)-4,4,10,13,14-pentamethyl-17-[(R)-6-methylheptan-2-yl]-4,5,6,7,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3(2H)-one O-methyl oxime 
• 108628-33-7 2-((Z)-benzylidene)-lanost-8-en-3-one 
• 40768-55-6 (5R,10S,13R,14R,17R)-3-Benzylsulfanyl-17-((R)-1,5-dimethyl-hexyl)-4,4,10,13,14-pentamethyl-4,5,6,7,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene 
• 131896-72-5 3β-benzoyloxy-lanost-8-ene 

1255-26-1Relevant articles and documents

-

Adam,G. et al.

, p. 3783 - 3788 (1969)

-

-

Bellamy,Doree

, p. 176,181 (1941)

-

Studies on Transition-metal Oxo and Nitrido Complexes. Part 9. Periodato and Tellurato Oxo-ruthenium Complexes as Organic Oxidants. X-Ray Crystal Structure of trans-NaK5*8H2O

El-Hendawy, Ahmed M.,Griffith, William P.,Piggott, Brian,Williams, David J.

, p. 1983 - 1988 (2007/10/02)

Salts of the anion trans-6-, earlier formulated as 6-, and of 6- have been prepared, and the X-ray crystal structure of the complex trans-NaK5*8H2O determined .Vibrational and electronic spectra for these diamagnetic 'ruthenyl' complexes are also reported.The periodato complexes function as overall six-electron oxidants in aqueous solution, converting primary alcohols to carboxylic acids and secondary alcohols to ketones; such reactions can be rendered catalytic if periodate is used as a co-oxidant.The tellurato complex functions as a two-electron oxidant for alcohols.

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