1-Chloro-4-(isocyanomethyl)benzene

Base Information

• Chemical Name: 1-Chloro-4-(isocyanomethyl)benzene
• CAS No.: 39546-47-9
• Molecular Formula: C8H6ClN
• Molecular Weight: 151.595
• Hs Code.: 2926909090
• DSSTox Substance ID: DTXSID20373884
• Nikkaji Number: J757.868G
• Wikidata: Q82162259
• Mol file: 39546-47-9.mol

Synonyms:1-chloro-4-(isocyanomethyl)benzene;4-Chlorobenzylisocyanide;39546-47-9;4-chlorobenzylisonitrile;4-chlorobenzyl isocyanide;SCHEMBL3538182;DTXSID20373884;UNRNSTIWJVLLMX-UHFFFAOYSA-N;1-Chloro-4-isocyanomethyl-benzene;4-chlorobenzylisocyanide, AldrichCPR;BBL021325;MFCD02664571;STK894034;AKOS005144148;GS-0304;FT-0639554;EN300-1983574

Chemical Property of 1-Chloro-4-(isocyanomethyl)benzene

Chemical Property:

• PSA: 0.00000
• LogP: 1.99000
• XLogP3: 2.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 151.0188769
• Heavy Atom Count: 10
• Complexity: 139

Purity/Quality:

98%min ^*data from raw suppliers

1-CHLORO-4-(ISOCYANOMETHYL)BENZENE 95 ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: [C-]#[N+]CC1=CC=C(C=C1)Cl

Technology Process of 1-Chloro-4-(isocyanomethyl)benzene

There total 7 articles about 1-Chloro-4-(isocyanomethyl)benzene 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: 98.0%

N-(4-chlorobenzyl)formamide (86386-67-6) → p-chlorobenzylisocyanide (39546-47-9)

Guidance literature:

With triethylamine; trichlorophosphate; In dichloromethane; at 0 ℃; Green chemistry;

DOI:10.1039/d0gc02722g

Reference yield: 93.0%

(4-chloro-benzyl)-(1(2)H-tetrazol-5-yl)-amine (31694-96-9) → p-chlorobenzylisocyanide (39546-47-9)

Guidance literature:

With sodium ethanolate; In ethanol; Electrolysis;

DOI:10.1021/acs.orglett.1c03475

Reference yield: 64.0%

chloroform (67-66-3,8013-54-5) + 4-chlorobenzylamine (104-86-9) → p-chlorobenzylisocyanide (39546-47-9)

Guidance literature:

With sodium hydroxide; N-benzyl-N,N,N-triethylammonium chloride; In dichloromethane; water; for 6h;

DOI:10.1016/S0040-4020(98)00104-5

upstream raw materials:

N-(4-chlorobenzyl)formamide

chloroform

4-chlorobenzylamine

trimethylsilyl cyanide

Downstream raw materials:

α-Isocyano-p-chlorphenylessigsaeureaethylester

2-[(5-iodo-6-methyl-2-phenylpyrimidin-4-yl)-(5-methylfuran-2-ylmethyl)-amino]-4-methylpentanoic acid 4-chlorobenzylamide

N-(4-chlorobenzyl)-2-[furan-2-ylmethyl-(5-iodo-2-isopropyl-6-methylpyrimidin-4-yl)-amino]-acetamide

N-(4-chlorobenzyl)-2-(4-chlorophenyl)-2-[(5-iodo-2-isopropyl-6-methylpyrimidin-4-yl)-(5-methylfuran-2-ylmethyl)-amino]-acetamide