(3R,6E)-nerolidol

Base Information

Chemical Name:(3R,6E)-nerolidol
CAS No.:17430-12-5
Molecular Formula:C₁₅H₂₆O
Molecular Weight:222.371
Hs Code.:
UNII:UOC0644V25
DSSTox Substance ID:DTXSID901338722
Metabolomics Workbench ID:60896
Nikkaji Number:J61.190E,J742.381K
Wikidata:Q27126989

Synonyms:(3R,6E)-nerolidol;77551-75-8;Nerolidol, (6E)-(-)-;(3R,6E)-3,7,11-trimethyldodeca-1,6,10-trien-3-ol;(3R)-(6E)-nerolidol;UOC0644V25;1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl-, (3R,6E)-;17430-12-5;(E)-nerolidol;trans-(R)-Nerolidol;UNII-UOC0644V25;(-)-Nerolidol;(e)-(r)-nerolidol;Nerolidol, (-)-;FEMA No. 2772, E-(-)-;(-)-(R)-Nerolidol;(3R)-(E)-nerolidol;(6E)-(-)-nerolidol;BIDD:ER0616;UNII-9A7Y7619GR;CHEBI:59959;9A7Y7619GR;DTXSID901338722;FEMA No. 2772, (-)-;C19746;Q27126989;(3R,6E)-3,7,11-Trimethyl-1,6,10-dodecatrien-3-ol;1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl-, (3R)-;28U

Suppliers and Price of (3R,6E)-nerolidol

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
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price

Total 0 raw suppliers

Chemical Property of (3R,6E)-nerolidol

Chemical Property:

XLogP3:4.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:7
Exact Mass:222.198365449
Heavy Atom Count:16
Complexity:269

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(=CCCC(=CCCC(C)(C=C)O)C)C
Isomeric SMILES:CC(=CCC/C(=C/CC[C@](C)(C=C)O)/C)C

Technology Process of (3R,6E)-nerolidol

There total 14 articles about (3R,6E)-nerolidol 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: 97.0%

: 85431-78-3
(2S,3S)-2-((E)-4,8-Dimethyl-nona-3,7-dienyl)-3-iodomethyl-2-methyl-oxirane

: 142-50-7,1119-38-6,2211-29-2,3790-78-1,7212-44-4,17430-12-5,35944-21-9,40716-66-3,53991-23-4,77171-59-6,132958-73-7,77551-75-8
(R)-(-)-trans-nerolidol

Guidance literature:: With zinc; In diethyl ether; acetic acid; for 1h; Ambient temperature;
DOI:10.1016/0040-4039(82)80144-5

Reference yield: 55.0%

: 85505-95-9
(2R,3R)-3-((E)-4,8-dimethylnona-3,7-dien-1-yl)-3-methyloxiran-2-yl-methanol

: 142-50-7,1119-38-6,2211-29-2,3790-78-1,7212-44-4,17430-12-5,35944-21-9,40716-66-3,53991-23-4,77171-59-6,132958-73-7,77551-75-8
(R)-(-)-trans-nerolidol

Guidance literature:: (2R,3R)-3-((E)-4,8-dimethylnona-3,7-dien-1-yl)-3-methyloxiran-2-yl-methanol; With pyridine; iodine; triphenylphosphine; In diethyl ether; acetonitrile; at 0 ℃; for 2h; Inert atmosphere;

With water; In diethyl ether; acetonitrile; for 12h; Reflux;
DOI:10.3762/bjoc.15.75

Reference yield:

: 372-97-4,13058-04-3,25744-33-6,27248-37-9,27248-38-0,40716-68-5
farnesyl pyrophosphate

: 18794-84-8
(E)-β-farnesene

: 38738-45-3
racemic zingiberene

: 159407-35-9
7‐epi‐sesquithujene

: 1431636-59-7
sesquisabinene B

: 495-61-4
(S)-1-methyl-4-(6-methylhepta-1,5-dien-2-yl)cyclohex-1-ene

: 72345-84-7
(+/-)-β-curcumene

: 1309585-05-4
(+)-(2S,6S,7S)-sesquithujene

: 53585-13-0
[E]-γ-bisabolene

: 13474-59-4,14087-02-6,17699-05-7,17829-53-7,18252-46-5,35334-58-8,64727-43-1,23971-87-1
trans‐α‐bergamotene

: 451-55-8
γ-curcumene

: sesquisabinene A

: 142-50-7,1119-38-6,2211-29-2,3790-78-1,7212-44-4,17430-12-5,35944-21-9,40716-66-3,53991-23-4,77171-59-6,132958-73-7,77551-75-8
(R)-(-)-trans-nerolidol

: 13474-59-4,14087-02-6,17699-05-7,17829-53-7,18252-46-5,23971-87-1,35334-58-8,64727-43-1
trans-α-bergamotene

Guidance literature:: With sodium tungstate; recombinant terpene synthases TPS₄-B₇₃ from Zea mays; sodium fluoride; magnesium chloride; In pentane; at 30 ℃; for 0.333333h; pH=7; Reagent/catalyst; Inert atmosphere; Enzymatic reaction;
DOI:10.1039/c4cc10395e