(1R,2R)-2-aminocyclohex-3-ene-1-carboxylic acid

Base Information

Chemical Name:(1R,2R)-2-aminocyclohex-3-ene-1-carboxylic acid
CAS No.:785015-46-5
Molecular Formula:C₇H₁₁NO₂
Molecular Weight:141.17
Hs Code.:
DSSTox Substance ID:DTXSID10420659
Mol file:785015-46-5.mol

Synonyms:785015-46-5;(1R,2R)-2-aminocyclohex-3-ene-1-carboxylic acid;DTXSID10420659;3-Cyclohexene-1-carboxylicacid,2-amino-,(1R-trans)-(9CI)

Suppliers and Price of (1R,2R)-2-aminocyclohex-3-ene-1-carboxylic 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

Total 1 raw suppliers

Chemical Property of (1R,2R)-2-aminocyclohex-3-ene-1-carboxylic acid

Chemical Property:

PSA：63.32000
LogP:1.06480
XLogP3:-1.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:141.078978594
Heavy Atom Count:10
Complexity:165

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC(C(C=C1)N)C(=O)O
Isomeric SMILES:C1C[C@H]([C@@H](C=C1)N)C(=O)O

Technology Process of (1R,2R)-2-aminocyclohex-3-ene-1-carboxylic acid

There total 25 articles about (1R,2R)-2-aminocyclohex-3-ene-1-carboxylic 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: 62.0%

: cis-6-carbomethoxy-2-cyclohexen-1-yl carbamate

: 193673-65-3,285560-96-5,285560-97-6,473835-79-9,785015-46-5
(1RS,2SR)-2-aminocyclohex-3-enecarboxylic acid

Guidance literature:: With trimethylsilyl iodide; In chloroform; at 55 ℃; for 12h;
DOI:10.1021/jm020134i

Reference yield: 57.0%

: trans-6-carbomethoxy-2-cyclohexen-1-yl carbamate

: 193673-65-3,285560-96-5,285560-97-6,473835-79-9,785015-46-5
trans-2-aminocyclohex-3-ene-1-carboxylic acid

Guidance literature:: With trimethylsilyl iodide; In chloroform; at 55 ℃; for 12h;
DOI:10.1021/jm020134i

Reference yield: 48.0%

: rac,cis-7-azabicyclo<4.2.0>-oct-4-en-8-one

: 285560-99-8
(1S,6R)-7-azabicyclo[4.2.0]oct-4-en-8-one

: 193673-65-3,285560-96-5,285560-97-6,473835-79-9,785015-46-5
(1R,2S)-cis-2-aminocyclohex-3-enecarboxylic acid

Guidance literature:: With Candida antarctica lipase B on resin; In di-isopropyl ether; water; at 70 ℃; for 5h;
DOI:10.1016/j.tetasy.2004.05.029