Benzyl (1S,3S)-3-hydroxycyclohexylcarbamate

Base Information Edit

Chemical Name:Benzyl (1S,3S)-3-hydroxycyclohexylcarbamate
CAS No.:750649-39-9
Molecular Formula:C₁₄H₁₉NO₃
Molecular Weight:249.31
Hs Code.:
DSSTox Substance ID:DTXSID201151755
Nikkaji Number:J2.075.397H
Mol file:750649-39-9.mol

Synonyms:750649-39-9;BENZYL (1S,3S)-3-HYDROXYCYCLOHEXYLCARBAMATE;Benzyl N-[(1S,3S)-3-hydroxycyclohexyl]carbamate;750649-44-6;Trans-3-N-CBZ-AMINOCYCLOHEXANOL;Benzyl ((1S,3S)-3-hydroxycyclohexyl)carbamate;MFCD23378488;DTXSID201151755;AM805558;BS-42592;CS-0036345;Benzyl((1S,3S)-3-hydroxycyclohexyl)carbamate;W11745;W19471;Carbamic acid, [(1R,3R)-3-hydroxycyclohexyl]-, phenylmethyl ester, rel-

Suppliers and Price of Benzyl (1S,3S)-3-hydroxycyclohexylcarbamate

Supply Marketing:Edit

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

Crysdot
Benzyl(trans-3-hydroxycyclohexyl)carbamate 95+%
5g
$ 1786.00

Crysdot
Benzyl(trans-3-hydroxycyclohexyl)carbamate 95+%
1g
$ 594.00

Chemenu
Benzyl(trans-3-hydroxycyclohexyl)carbamate 95%
1g
$ 561.00

Absolute Chiral
transbenzyl(3-hydroxycyclohexyl)carbamate 97%
250 mg
$ 598.00

Absolute Chiral
transbenzyl(3-hydroxycyclohexyl)carbamate 97%
100 mg
$ 298.00

Total 5 raw suppliers

Chemical Property of Benzyl (1S,3S)-3-hydroxycyclohexylcarbamate Edit

Chemical Property:

XLogP3:2.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:249.13649347
Heavy Atom Count:18
Complexity:264

Purity/Quality:

99% ^*data from raw suppliers

Benzyl(trans-3-hydroxycyclohexyl)carbamate 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CC(CC(C1)O)NC(=O)OCC2=CC=CC=C2
Isomeric SMILES:C1C[C@@H](C[C@H](C1)O)NC(=O)OCC2=CC=CC=C2

Technology Process of Benzyl (1S,3S)-3-hydroxycyclohexylcarbamate

There total 45 articles about Benzyl (1S,3S)-3-hydroxycyclohexylcarbamate 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: 97.4%