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24684-41-1

24684-41-1

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24684-41-1 Usage

Type of compound

Synthetic opiate and opioid analgesic

Chemical structure

Closely related to morphine

Mechanism of action

Acts on the central nervous system to produce potent pain relief and sedation

Medical use

Treatment of severe pain

Derivative

Morphine

Potential for addiction

High, similar to morphine

Legal classification

Schedule I controlled substance in the United States

Risks

Addiction, abuse, respiratory depression, and overdose

Precaution

Should only be used under strict medical supervision

Check Digit Verification of cas no

The CAS Registry Mumber 24684-41-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,6,8 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 24684-41:
(7*2)+(6*4)+(5*6)+(4*8)+(3*4)+(2*4)+(1*1)=121
121 % 10 = 1
So 24684-41-1 is a valid CAS Registry Number.
InChI:InChI=1/C18H16/c1-12-11-14-6-4-8-15(14)17-10-9-13-5-2-3-7-16(13)18(12)17/h2-3,5,7,9-11H,4,6,8H2,1H3

24684-41-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 11-methyl-16,17-dihydro-15H-cyclopenta[a]phenanthrene

1.2 Other means of identification

Product number -
Other names 4-Methyl-1,2-cyclopentenophenanthrene

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:24684-41-1 SDS

24684-41-1Relevant articles and documents

α-Oxoketene dithioacetal mediated aromatic annulation: Highly efficient and concise synthetic routes to potentially carcinogenic polycyclic aromatic hydrocarbons

Nandi, Sukumar,Panda, Kausik,Suresh,Ila, Hiriyakkanavar,Junjappa, Hiriyakkanavar

, p. 3663 - 3673 (2007/10/03)

Highly efficient regiospecific routes to potentially carcinogenic polycyclic aromatic hydrocarbons such as substituted benzo[c]phenanthrenes, benzo[c]fluorenes, 16,17-dihydro-11-methyl-15[H]cyclopenta[a]phenanthrene, 5-methyl-7,8,9,10-tetrahydrochrysene and 1,4-dimethylphenanthrene have been developed. The overall strategy involves our aromatic annulation protocol through base induced conjugate addition-elimination on the cyclic and acyclic α-oxoketene dithioacetals with the appropriate arylacetonitriles followed by acid induced cyclodehydration of the resulting conjugate adducts. Subsequent reductive dethiomethylation (Raney Ni) and dehydrogenation (DDQ) of the cyclized products affords the methyl substituted PAHs in high yields.

A NEW SYNTHESIS OF CYCLOPENTA PHENANTHRENE AND ITS CARCINOGENIC DERIVATIVES

Lee, Homgmee,Harvey, Roland G.

, p. 3207 - 3210 (2007/10/02)

A novel synthesis of ciclopenta phenanthrene and its carcinogenic 11-methyl and 17-keto derivatives is described.

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