N-ethylcarbamoyl chloride

Base Information

• Chemical Name: N-ethylcarbamoyl chloride
• CAS No.: 41891-13-8
• Molecular Formula: C3H6ClNO
• Molecular Weight: 107.54
• Hs Code.: 2903199000
• European Community (EC) Number: 816-004-8
• DSSTox Substance ID: DTXSID60488724
• Nikkaji Number: J94.722I
• Wikidata: Q82331569
• Mol file: 41891-13-8.mol

Synonyms:N-ethylcarbamoyl chloride;41891-13-8;Carbamic chloride, ethyl-;Carbamicchloride,ethyl-;ethylcarbamyl chloride;Carbamic chloride,ethyl-;SCHEMBL2041739;DTXSID60488724;PJLHXSBKGRJXHA-UHFFFAOYSA-N;N-Ethylcarbamoyl Chloride (>90%);AKOS006349302;FT-0739013;EN300-123440

Chemical Property of N-ethylcarbamoyl chloride

Chemical Property:

• PSA: 29.10000
• LogP: 1.34560
• XLogP3: 1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 107.0137915
• Heavy Atom Count: 6
• Complexity: 54.8

Purity/Quality:

99% ^*data from raw suppliers

N-EthylcarbamoylChloride(>90%) ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCNC(=O)Cl

Technology Process of N-ethylcarbamoyl chloride

There total 6 articles about N-ethylcarbamoyl chloride 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:

S-methyl N-ethylthiocarbamate (39076-43-2) → ethyl carbamoyl chloride (41891-13-8)

Guidance literature:

With chlorine; In Dimethyldisulphide; at -15 - -10 ℃;

DOI:10.1055/s-2008-1072573

Reference yield:

S-ethyl N-ethylthiocarbamate (39078-37-0) → ethyl carbamoyl chloride (41891-13-8)

Guidance literature:

With benzenesulfenyl chloride;

DOI:10.1021/jo00350a092

Reference yield:

ethyl isocyanate (109-90-0) → ethyl carbamoyl chloride (41891-13-8)

Guidance literature:

With hydrogenchloride;

upstream raw materials:

phosgene

ethanamine hydrochloride

ethyl isocyanate

S-ethyl N-ethylthiocarbamate

Downstream raw materials:

N-ethyl-4-methyl-1-piperazinecarboxamide

N-(ethylcarbamoyl)benzenesulfonamide

N-ethylbenzamide

ethyl isocyanate

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