Hydrocyanic acid-D

Base Information

• Chemical Name: Hydrocyanic acid-D
• CAS No.: 3017-23-0
• Molecular Formula: CD N
• Molecular Weight: 28.0177
• DSSTox Substance ID: DTXSID80184251
• Nikkaji Number: J298.921B
• Wikidata: Q81977224
• Mol file: 3017-23-0.mol

Synonyms:3017-23-0;HYDROCYANIC ACID-D;Hydrogen-d cyanide;deuterium cyanide;Hydrocyanic-d acid;Hydrogen cyanide-d1;deuterohydrocyanic acid;DTXSID80184251

Chemical Property of Hydrocyanic acid-D

Chemical Property:

• Vapor Pressure: 740mmHg at 25°C
• Boiling Point: 25.7°Cat760mmHg
• Flash Point: °C
• PSA: 23.79000
• Density: 0.72g/cm³
• LogP: 0.13978
• XLogP3: 0.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 28.017175782
• Heavy Atom Count: 2
• Complexity: 10

Purity/Quality:

98%min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C#N
• Isomeric SMILES: [2H]C#N

Technology Process of Hydrocyanic acid-D

There total 12 articles about Hydrocyanic acid-D which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

fulminic acid (51060-05-0,20411-61-4) → isocyanic acid (75-13-8) + hydrogen cyanide (74-90-8) + hydrogen cyanide (3017-23-0) + carbon monoxide (201230-82-2) + CO(18)O (18983-82-9)

Guidance literature:

With nitric oxide; nitric oxide; ethane-d6; cyclohexane; at 24.84 ℃; under 0.1 Torr; Reagent/catalyst; Quantum yield; Kinetics; Photolysis;

DOI:10.1016/j.chemphys.2016.02.017

Reference yield:

fulminic acid (51060-05-0,20411-61-4) + ethane-d6 (1632-99-1) + H2(15)N(18)O (15917-79-0) + oxygen-18 (32767-18-3) → imino radical (13774-92-0) + isocyanic acid (75-13-8) + hydrogen cyanide (74-90-8) + hydrogen cyanide (3017-23-0) + carbon monoxide (201230-82-2) + carbon monoxide (55125-78-5) + CO(18)O (18983-82-9)

Guidance literature:

at 24.84 ℃; Photolysis;

DOI:10.1021/jp411209n

Reference yield:

carbon nitride (2074-87-5) + chloroform-d1 (865-49-6) → trichloromethyl radical (3170-80-7) + hydrogen cyanide (3017-23-0) + dichloromethane-d1 (1665-01-6) + cyanogen chloride (506-77-4)

Guidance literature:

at 24.84 ℃; Kinetics;

DOI:10.1016/j.cplett.2008.06.014

upstream raw materials:

Benz-aldehyd-isobutylimid

deuterated methyl radical

carbon nitride

chloroform-d1

Downstream raw materials:

trans-4-t-butyl(2-D)cyclohexanecarbonitrile

cis-3-t-butyl(6-D)cyclohexanecarbonitrile

(E)-3-phenyl(3-D)prop-2-enenitrile

hydrogen cyanide

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