2-tert-ButyloxycarbonylaMino-5-heptenoic Acid

Base Information

Chemical Name:2-tert-ButyloxycarbonylaMino-5-heptenoic Acid
CAS No.:119808-36-5
Molecular Formula:C12H21NO4
Molecular Weight:243.29900
Hs Code.:
Mol file:119808-36-5.mol

Synonyms:2-tert-Butyloxycarbonylamino-5-heptenoic Acid;

Suppliers and Price of 2-tert-ButyloxycarbonylaMino-5-heptenoic Acid

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

TRC
2-tert-Butyloxycarbonylamino-5-heptenoicAcid
25mg
$ 180.00

Medical Isotopes, Inc.
2-tert-Butyloxycarbonylamino-5-heptenoicAcid
250 mg
$ 2400.00

Medical Isotopes, Inc.
2-tert-Butyloxycarbonylamino-5-heptenoicAcid
25 mg
$ 675.00

AK Scientific
2-Tert-butoxycarbonylamino-hept-6-enoicacid
500mg
$ 532.00

Activate Scientific
2-(Boc-amino)-6-heptenoic acid 95+%
1 g
$ 674.00

Activate Scientific
2-(Boc-amino)-6-heptenoic acid 95+%
250 mg
$ 308.00

Acrotein
2-(Boc-amino)-6-heptenoicacid 97%
0.5g
$ 330.00

Total 3 raw suppliers

Chemical Property of 2-tert-ButyloxycarbonylaMino-5-heptenoic Acid

Chemical Property:

Melting Point:68-70oC
PSA：75.63000
LogP:2.71150
Storage Temp.:-20°C Freezer
Solubility.:Chloroform (Slightly), Methanol (Slightly)

Purity/Quality:

99% ^*data from raw suppliers

2-tert-Butyloxycarbonylamino-5-heptenoicAcid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses 2-tert-ButyloxycarbonylaMino-5-heptenoic Acid is a reactant used in the preparation of (-)-Amathaspiramide F.

Technology Process of 2-tert-ButyloxycarbonylaMino-5-heptenoic Acid

There total 1 articles about 2-tert-ButyloxycarbonylaMino-5-heptenoic Acid 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: 94.0%

: 1150697-18-9
ethyl 2-tert-butoxycarbonylamino-hept-6-enoate

: 119808-36-5
2-tert-butoxycarbonylamino-hept-6-enoic acid

Guidance literature:: With lithium hydroxide monohydrate; water; In ethanol; at 0 ℃;
DOI:10.1021/jm900125m

Reference yield: 67.0%

: 119808-36-5
2-tert-butoxycarbonylamino-hept-6-enoic acid

: 62-53-3
aniline

: 1150697-21-4
tert-butyl 1-(phenylaminocarbonyl)hex-5-en-1-ylcarbamate

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In water; N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1021/jm900125m

Reference yield:

: 119808-36-5
2-tert-butoxycarbonylamino-hept-6-enoic acid

: 139-59-3
4-phenoxyanilin

: 1150697-34-9
C₂₄H₃₀N₂O₄

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In water; N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1021/jm900125m