Tert-butyl m-tolylcarbamate

Base Information

Chemical Name:Tert-butyl m-tolylcarbamate
CAS No.:18437-67-7
Molecular Formula:C12H17NO2
Molecular Weight:207.272
Hs Code.:2924299090
DSSTox Substance ID:DTXSID80406844
Nikkaji Number:J1.604.030D
Wikidata:Q82211959
Mol file:18437-67-7.mol

Synonyms:tert-butyl m-tolylcarbamate;18437-67-7;tert-butyl N-(3-methylphenyl)carbamate;tert-Butylm-tolylcarbamate;SCHEMBL8966117;DTXSID80406844;MFCD07127701;AKOS003581109;SB77828;AM805972;BS-15668;CS-0152987;FT-0705455;A849982;J-524792

Suppliers and Price of Tert-butyl m-tolylcarbamate

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
Packaging
price

Matrix Scientific
tert-Butyl m-tolylcarbamate 95%
1g
$ 104.00

Matrix Scientific
tert-Butyl m-tolylcarbamate 95%
5g
$ 322.00

Crysdot
tert-Butylm-tolylcarbamate 95+%
25g
$ 564.00

American Custom Chemicals Corporation
TERT-BUTYL-META-TOLYLCARBAMATE 95.00%
5MG
$ 501.75

Ambeed
tert-Butylm-tolylcarbamate 98%
5g
$ 143.00

Ambeed
tert-Butylm-tolylcarbamate 98%
1g
$ 46.00

Ambeed
tert-Butylm-tolylcarbamate 98%
250mg
$ 16.00

Alichem
tert-Butylm-tolylcarbamate
25g
$ 598.50

Total 14 raw suppliers

Chemical Property of Tert-butyl m-tolylcarbamate

Chemical Property:

PSA：41.82000
LogP:3.35560
Storage Temp.:Sealed in dry,Room Temperature
XLogP3:3.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:207.125928785
Heavy Atom Count:15
Complexity:220

Purity/Quality:

97% ^*data from raw suppliers

tert-Butyl m-tolylcarbamate 95% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC(=CC=C1)NC(=O)OC(C)(C)C

Technology Process of Tert-butyl m-tolylcarbamate

There total 5 articles about Tert-butyl m-tolylcarbamate 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: 100.0%

: 24424-99-5
di-tert-butyl dicarbonate

: 108-44-1
1-amino-3-methylbenzene

: 18437-67-7
1,1-dimethylethyl (3-methylphenyl)carbamate

Guidance literature:: copper(II) bis(tetrafluoroborate); at 30 - 33 ℃; for 0.25h;
DOI:10.1016/j.tetlet.2005.12.044

Reference yield: 94.0%

: 4248-19-5
tert-butyl carbazate

: 591-17-3
meta-bromotoluene

: 18437-67-7
1,1-dimethylethyl (3-methylphenyl)carbamate

Guidance literature:: With bis[chloro(1,2,3-trihapto-allylbenzene)palladium(II)]; potassium hydroxide; tert-butyl XPhos; In ethanol; at 50 ℃; for 6h;
DOI:10.1021/acscatal.1c04641