(1S,2S)-2-Phenylcyclohexane-1-carbaldehyde

Base Information

Chemical Name:(1S,2S)-2-Phenylcyclohexane-1-carbaldehyde
CAS No.:218938-79-5
Molecular Formula:C13H16O
Molecular Weight:188.269
Hs Code.:
DSSTox Substance ID:DTXSID20574031
Nikkaji Number:J1.664.588E
Wikidata:Q82462909
Mol file:218938-79-5.mol

Synonyms:(1S,2S)-2-Phenylcyclohexane-1-carbaldehyde;218938-79-5;DTXSID20574031

Suppliers and Price of (1S,2S)-2-Phenylcyclohexane-1-carbaldehyde

Supply Marketing:

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

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Chemical Property of (1S,2S)-2-Phenylcyclohexane-1-carbaldehyde

Chemical Property:

XLogP3:3.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:188.120115130
Heavy Atom Count:14
Complexity:182

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCC(C(C1)C=O)C2=CC=CC=C2
Isomeric SMILES:C1CC[C@@H]([C@H](C1)C=O)C2=CC=CC=C2

Technology Process of (1S,2S)-2-Phenylcyclohexane-1-carbaldehyde

There total 6 articles about (1S,2S)-2-Phenylcyclohexane-1-carbaldehyde 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: 73.0%

: 396718-86-8
Acetic acid (1R,2R)-1,2-diphenyl-2-[(R)-2-phenyl-cyclohex-(E)-ylidenemethoxy]-ethyl ester

: 218938-79-5
2-Phenylcyclohexanecarboxaldehyde

Guidance literature:: Acetic acid (1R,2R)-1,2-diphenyl-2-[(R)-2-phenyl-cyclohex-(E)-ylidenemethoxy]-ethyl ester; With formic acid; In pentane; for 2h;

With sodium hydroxide; for 0.25h;
DOI:10.1016/S0957-4166(01)00319-6

Reference yield:

: 62134-74-1
N-(1-cyclohexenylmethylidene)cyclohexylamine

: 591-51-5
phenyllithium

: 218938-79-5
2-Phenylcyclohexanecarboxaldehyde

Guidance literature:: With acetate buffer; acetate buffer (ph 4.5); (1R,2R)-1,2-diphenyl-1,2-dimethoxyethane; Yield given. Multistep reaction; 1.) toluene, -45 deg C, 7 h; 2.) 12 h;
DOI:10.1021/ja00203a032

Reference yield:

: 1192-88-7
1-cyclohexene-1-carboxaldehyde

: 218938-79-5
2-Phenylcyclohexanecarboxaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / 4 Angstroems MS / hexane / 48 h

2: 1.) (1R,2R)-1,2-dimethoxy-1,2-diphenylethane, 2.) acetate buffer / 1.) toluene, -45 deg C, 3 h, 2.) H₂O, toluene, rt, 1.5 h

With acetate buffer; 4 Angstroems MS; (1R,2R)-1,2-diphenyl-1,2-dimethoxyethane; In hexane;
DOI:10.1021/jo9813181