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  • 123123-41-1 Structure
  • Basic information

    1. Product Name: capsimine
    2. Synonyms: capsimine
    3. CAS NO:123123-41-1
    4. Molecular Formula: C27H45NO2
    5. Molecular Weight: 415.6517
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 123123-41-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 544.2°Cat760mmHg
    3. Flash Point: 59°C
    4. Appearance: /
    5. Density: 1.09g/cm3
    6. Vapor Pressure: 4.09E-14mmHg at 25°C
    7. Refractive Index: 1.563
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: capsimine(CAS DataBase Reference)
    11. NIST Chemistry Reference: capsimine(123123-41-1)
    12. EPA Substance Registry System: capsimine(123123-41-1)
  • 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: 123123-41-1(Hazardous Substances Data)

123123-41-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123123-41-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,1,2 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 123123-41:
(8*1)+(7*2)+(6*3)+(5*1)+(4*2)+(3*3)+(2*4)+(1*1)=71
71 % 10 = 1
So 123123-41-1 is a valid CAS Registry Number.
InChI:InChI=1/C27H45NO2/c1-16-5-8-23(28-15-16)17(2)25-24(30)14-22-20-7-6-18-13-19(29)9-11-26(18,3)21(20)10-12-27(22,25)4/h6,16-17,19-25,28-30H,5,7-15H2,1-4H3/t16-,17-,19+,20-,21+,22+,23-,24-,25?,26+,27+/m1/s1

123123-41-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,8S,9S,10R,13S,14S,16R)-10,13-dimethyl-17-[(1S)-1-[(2R,5R)-5-methylpiperidin-2-yl]ethyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,16-diol

1.2 Other means of identification

Product number -
Other names 16,28-Secosolanid-5-ene-3,16-diol,(3beta,16alpha,25beta)

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:123123-41-1 SDS

123123-41-1Relevant articles and documents

Partial Synthesis of the Steroid Alkaloids Teinemine, 22-Isoteinemine, Etioline, and 25-Isoetioline

Quyen, Le thi,Ripperger, Helmut,Schreiber, Klaus

, p. 143 - 149 (2007/10/02)

The rare 16α-hydroxylated steroid alkaloids teinemine , 22-isoteinemine , etioline , and 25-isoetioline are synthesized from the abundant spirosolane alkaloids tomatid-5-en-3β-ol and solasodine , respectively.The crucial stages of these syntheses are the conversion of 1 or 15 into the N-protected (22S,25S)-, (22R,25S)-, and (22S,25R) -22,26-epimino-3β-hydroxycholest-5-en-16-ones 6, 7, and 18 as well as their reductions with sodium/2-propanol to the 16α-hydroxy compounds teinemine (8), 22-isoteinemine (10), and (22S,25R)-22,26-epiminocholest-5-ene-3β,16α-diol (19), respectively.By treatment with sodium methanolate the N-chloro derivatives 9 and 11 of 8 and 10 afford etioline (12).In an analogous manner, the N-chloro derivative 20 of 19 is converted into 25-isoetioline (21).

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