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62472-39-3

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62472-39-3 Usage

General Description

Tricyclo[3.3.1.1(3,7)]decane-1,3-dicarboxamide is a chemical compound with a unique cage-like structure consisting of three fused cyclohexane rings. It is commonly used as a building block in organic synthesis and is known for its stability and rigidity. Tricyclo[3.3.1.1(3,7)]decane-1,3-dicarboxamide has potential applications in materials science and drug discovery due to its ability to bind to molecules and form stable complexes. Its unique structure makes it a valuable tool in the development of new chemical reactions and molecular designs. Additionally, its high level of symmetry and stability make it an attractive target for research into new materials and potential drug candidates.

Check Digit Verification of cas no

The CAS Registry Mumber 62472-39-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,7 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 62472-39:
(7*6)+(6*2)+(5*4)+(4*7)+(3*2)+(2*3)+(1*9)=123
123 % 10 = 3
So 62472-39-3 is a valid CAS Registry Number.
InChI:InChI=1S/C12H18N2O2/c13-9(15)11-2-7-1-8(4-11)5-12(3-7,6-11)10(14)16/h7-8H,1-6H2,(H2,13,15)(H2,14,16)

62472-39-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name adamantane-1,3-dicarboxamide

1.2 Other means of identification

Product number -
Other names 1,3-disaminoacyladamantane

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:62472-39-3 SDS

62472-39-3Relevant articles and documents

X-ray structure of 1,3-adamantane dicarbonamide

Bridson, John N.,Schriver, Melbourne J.,Zhu, Shuguang

, p. 11 - 14 (1995)

The X-ray crystal structure of 1,3-adamantane-dicarbonamide has been determined.Colourless, sube shaped crystals of C12H18N2O2 crystallize in the monoclinic space group C2/c (15) with cell dimensions a = 7*934(3), b = 15*543(3), c = 9*404(2) Angstroem, β = 93.63 deg; V = 1157.4(5) Angstroem3 and Z = 4. 1074 unique reflections with Inet > 2.00?(I) on refinement afforded values of R = 0.039 and Rw = 0.040. Key words: Adamantane, dicarbonamide, structure

Corresponding amine nitrile and method of manufacturing thereof

-

Paragraph 0125; 0127, (2017/10/22)

The invention relates to a preparation method of nitrile. Compared with the prior art, the preparation method has the characteristics of obvious reduction of the usage amount of ammonia sources, low environmental pressure, low energy consumption, low production cost, high purity and yields of nitrile products, and the like, and can be used for obtaining nitrile with a more complex structure. The invention also relates to a method for preparing corresponding amine with nitrile.

Efficient synthesis of 1,3-adamantanedicarboxylic acid and 1,3-diaminoadamantane

Zhu, Hua,Zhong, Xin

, p. 4119 - 4120 (2013/06/04)

1,3-Adamantane dicarboxylic acid was efficiently synthesized from 1-adamantane carboxylic acid by one-pot method. 1,3- Diaminoadamantane was synthesized from 1,3-adamantane dicarboxylic acid via amidation reaction and Hofmann degradation. The structure was confirmed by NMR spectra, etc.

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