3-endo-Hydroxycamphor

Base Information

Chemical Name:3-endo-Hydroxycamphor
CAS No.:28357-09-7
Molecular Formula:C₁₀H₁₆O₂
Molecular Weight:168.236
Hs Code.:
UNII:2WMW6SF9QS
Nikkaji Number:J676.194A

Synonyms:3-endo-Hydroxycamphor;2WMW6SF9QS;UNII-2WMW6SF9QS;3-Hydroxycamphor, (1R-endo-(-))-;2-Bornanone, 3-hydroxy-, (1R,3S,4S)-;28357-09-7;Bicyclo(2.2.1)heptan-2-one, 3-hydroxy-1,7,7-trimethyl-, (1R-endo)-;Bicyclo(2.2.1)heptan-2-one, 3-hydroxy-1,7,7-trimethyl-, (1R,3S,4S)-

Suppliers and Price of 3-endo-Hydroxycamphor

Supply Marketing:

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

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Chemical Property of 3-endo-Hydroxycamphor

Chemical Property:

XLogP3:1.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:168.115029749
Heavy Atom Count:12
Complexity:244

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1(C2CCC1(C(=O)C2O)C)C
Isomeric SMILES:C[C@@]12CC[C@@H](C1(C)C)[C@@H](C2=O)O

Technology Process of 3-endo-Hydroxycamphor

There total 19 articles about 3-endo-Hydroxycamphor 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: 95.0%

: 15795-31-0,31658-22-7,31658-57-8,83462-15-1,91839-98-4,125409-78-1
Acetic acid (1S,4R)-4,7,7-trimethyl-3-oxo-bicyclo[2.2.1]hept-2-yl ester

: 10373-81-6,21488-68-6,22759-33-7,24326-34-9,28357-09-7,28357-11-1,80513-77-5,80513-78-6,82264-38-8
3-hydroxycamphor

Guidance literature:: With potassium hydroxide; In methanol;
DOI:10.1016/S0040-4020(01)89491-6

Reference yield:

: 464-49-3,68546-28-1
(1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one

: 107438-74-4,1126-88-1,1607-84-7,4367-83-3,13948-58-8,22285-79-6
5-endo-hydroxy-1,7,7-trimethylbicyclo<2.2.1>heptan-2-one

: 28357-11-1
(+)-3R-exo-hydroxycamphor

: 10373-81-6,21488-68-6,22759-33-7,24326-34-9,28357-11-1,80513-77-5,80513-78-6,82264-38-8,28357-09-7
(-)-(3S)-endo-hydroxycamphor

Guidance literature:: With cindoxin; Escherichia coli flavodoxin reductase; N₂₄₂T mutant; NADPH; catalase; In aq. buffer; at 25 ℃; for 0.5h; Enzymatic reaction;
DOI:10.1016/j.abb.2019.07.025

Reference yield:

: 464-48-2,68546-28-1
(1S)-camphor

: 28357-11-1
(+)-3R-exo-hydroxycamphor

: 10373-81-6,21488-68-6,22759-33-7,24326-34-9,28357-11-1,80513-77-5,80513-78-6,82264-38-8,28357-09-7
(-)-(3S)-endo-hydroxycamphor

: (1S,2R)-1-methyl-2-hydroxy-7,7-dimethyl-bicyclo[2.2.1]hept-6-one

Guidance literature:: With cindoxin; Escherichia coli flavodoxin reductase; N₂₄₂T mutant; NADPH; catalase; In aq. buffer; at 25 ℃; for 0.5h; Enzymatic reaction;
DOI:10.1016/j.abb.2019.07.025