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111917-14-7

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111917-14-7 Usage

Molecular structure

A complex and unique structure, which is a derivative of tetrahydro-1H,4H-3a,6a-propanopentalene with a methylidene group.

Type of compound

Organic compound.

Potential applications

Building block in organic synthesis and use in medicinal chemistry.

Reactivity

Not widely studied, further research needed to understand its potential uses.

Molecular weight

136.24 g/mol (calculated from the molecular formula).

Stereochemistry

3a,6a-dihydro (indicates two hydrogen atoms are present in the 3a and 6a positions of the molecule).

Presence of functional groups

Methylidene group (a carbon-carbon double bond with a methyl group attached to one of the carbons).

Check Digit Verification of cas no

The CAS Registry Mumber 111917-14-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,9,1 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 111917-14:
(8*1)+(7*1)+(6*1)+(5*9)+(4*1)+(3*7)+(2*1)+(1*4)=97
97 % 10 = 7
So 111917-14-7 is a valid CAS Registry Number.

111917-14-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [3.3.3]Propellane, 2-methylene-

1.2 Other means of identification

Product number -
Other names (3.3.3)-Propellane,2-methylene

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:111917-14-7 SDS

111917-14-7Downstream Products

111917-14-7Relevant articles and documents

Synthesis of Propellanes by 'Exocyclic' Transannular Cycloaddition of Olefinic Methylenecyclopropanes

Yamago, Shigeru,Nakamura, Eiichi

, p. 1112 - 1113 (1988)

Olefinic methylenecyclopropanes undergo quantitative transannular ring closure under catalysis by Group 10 metals to give propellanes, through cycloaddition of a trimethylenemethane-like intermediate.

Antiproliferating polyquinanes. V. Di-and triquinanes involving alpha-methylene or alpha-alkylidene cyclopentanone, cyclopentenone, and gamma-lactone systems.

Kakiuchi,Ue,Takeda,Tadaki,Kato,Nagashima,Tobe,Koike,Ida,Odaira

, p. 617 - 631 (2007/10/02)

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