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CAS

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29782-28-3

(1α,6α)-7,7-Norcaranedicarbonitrile is a norcarane derivative with the molecular formula C8H9N. It is a bicyclic compound featuring a unique carbon framework and contains a carbon triple-bonded to a nitrogen atom, classifying it as a nitrile. This chemical may have potential applications in organic synthesis and material science, although its specific uses and properties are not extensively documented in the literature. Further research and characterization could uncover its potential applications across various industries.

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  • 29782-28-3 Structure

  • Basic information

    1. Product Name: (1α,6α)-7,7-Norcaranedicarbonitrile
    2. Synonyms: (1α,6α)-7,7-Norcaranedicarbonitrile
    3. CAS NO:29782-28-3
    4. Molecular Formula: C9H10N2
    5. Molecular Weight: 146.1891
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 29782-28-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (1α,6α)-7,7-Norcaranedicarbonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1α,6α)-7,7-Norcaranedicarbonitrile(29782-28-3)
    11. EPA Substance Registry System: (1α,6α)-7,7-Norcaranedicarbonitrile(29782-28-3)

  • 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: 29782-28-3(Hazardous Substances Data)

29782-28-3 Usage

Uses

Used in Organic Synthesis:
(1α,6α)-7,7-Norcaranedicarbonitrile is used as a synthetic intermediate for the development of various organic compounds. Its unique carbon framework and nitrile group provide opportunities for the creation of novel molecules with potential applications in different fields.
Used in Material Science:
(1α,6α)-7,7-Norcaranedicarbonitrile is utilized as a component in the research and development of new materials. Its distinctive structure and properties may contribute to the advancement of materials with specific characteristics, such as improved strength, flexibility, or chemical resistance, depending on the industry's requirements.
Note: The specific applications and industries for (1α,6α)-7,7-Norcaranedicarbonitrile are not detailed in the provided materials. The above uses are inferred based on its potential role in organic synthesis and material science. Further research would be necessary to identify concrete applications and industries where (1α,6α)-7,7-Norcaranedicarbonitrile could be utilized.

Check Digit Verification of cas no

The CAS Registry Mumber 29782-28-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,7,8 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 29782-28:
(7*2)+(6*9)+(5*7)+(4*8)+(3*2)+(2*2)+(1*8)=153
153 % 10 = 3
So 29782-28-3 is a valid CAS Registry Number.

29782-28-3SDS

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 7,7-Dicyan-norcaran

1.2 Other means of identification

Product number -
Other names 7,7-Dicyanonorcaran

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:29782-28-3 SDS

29782-28-3Relevant articles and documents

Asymmetric Catalysis by Vitamin B12: The Isomerization of Achiral Cyclopropanes to Optically Active Olefins

Troxler, Thomas,Scheffold, Rolf

, p. 1193 - 1202 (2007/10/02)

Achiral spiroactivated cyclopropanes are isomerized to optically active (R)-(cycloalk-2-enyl)-Meldrum's acids (= (R)-5-(cycloalk-2-enyl)-2,2-dimethyl-1,3-dioxane-4,6-diones) in high yield and ee's up to 86percent by catalytic amounts of cob(I)alamin in po

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