1-Tert-butyl-3-(2-chlorobenzyl)urea

Base Information

Chemical Name:1-Tert-butyl-3-(2-chlorobenzyl)urea
CAS No.:5768-95-6
Molecular Formula:C12H17ClN2O
Molecular Weight:240.7292
Hs Code.:
NSC Number:204281
DSSTox Substance ID:DTXSID90308466
Wikidata:Q82056364

Synonyms:5768-95-6;NSC204281;ST030740;DTXSID90308466;AKOS003809509;NSC-204281;1-TERT-BUTYL-3-(2-CHLOROBENZYL)UREA;N-(TERT-BUTYL)-N'-(2-CHLOROBENZYL)UREA

Suppliers and Price of 1-Tert-butyl-3-(2-chlorobenzyl)urea

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 0 raw suppliers

Chemical Property of 1-Tert-butyl-3-(2-chlorobenzyl)urea

Chemical Property:

Vapor Pressure:6.59E-07mmHg at 25°C
Boiling Point:409.2°Cat760mmHg
Flash Point:201.3°C
Density:1.119g/cm³
XLogP3:2.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:240.1029409
Heavy Atom Count:16
Complexity:238

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)NC(=O)NCC1=CC=CC=C1Cl

Technology Process of 1-Tert-butyl-3-(2-chlorobenzyl)urea

There total 7 articles about 1-Tert-butyl-3-(2-chlorobenzyl)urea 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:

: 176-80-7
1-azaspiro[4.5]decane

: 5768-95-6
10-[2-(1-aza-spiro[4.5]dec-1-yl)-ethyl]-10H-phenothiazine

Guidance literature:: Multi-step reaction with 3 steps

1: 150 °C

2: benzene; hydrogen chloride / anschliessend Behandeln mit Thionylchlorid

With hydrogenchloride; benzene;
DOI:10.1021/ja01569a052

Reference yield:

: 100049-37-4
2-(1-aza-spiro[4.5]dec-1-yl)-ethanol

: 5768-95-6
10-[2-(1-aza-spiro[4.5]dec-1-yl)-ethyl]-10H-phenothiazine

Guidance literature:: Multi-step reaction with 2 steps

1: benzene; hydrogen chloride / anschliessend Behandeln mit Thionylchlorid

With hydrogenchloride; benzene;
DOI:10.1021/ja01569a052

Reference yield:

: 5498-74-8
2-oxo-1-azaspiro<4.5>decane

: 5768-95-6
10-[2-(1-aza-spiro[4.5]dec-1-yl)-ethyl]-10H-phenothiazine

Guidance literature:: Multi-step reaction with 4 steps

1: lithium alanate; tetrahydrofuran

2: 150 °C

3: benzene; hydrogen chloride / anschliessend Behandeln mit Thionylchlorid

With tetrahydrofuran; hydrogenchloride; lithium aluminium tetrahydride; benzene;
DOI:10.1021/ja01569a052