Hopane

Base Information Edit

Chemical Name:Hopane
CAS No.:471-62-5
Molecular Formula:C₃₀H₅₂
Molecular Weight:412.743
Hs Code.:2929101000
UNII:W2H93796GT
DSSTox Substance ID:DTXSID00904337
Nikkaji Number:J12.030H
Wikipedia:Hopane
Wikidata:Q5898987
Metabolomics Workbench ID:55388
Mol file:471-62-5.mol

Synonyms:hopane;hopane, (17alpha)-isomer;hopane, (21beta)-isomer

Suppliers and Price of Hopane

Supply Marketing:Edit

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

Sigma-Aldrich
17β(H),21β(H)-Hopane solution 0.1?mg/mL in isooctane, analytical standard
1ml
$ 968.00

American Custom Chemicals Corporation
17BETA(H), 21BETA(H)-HOPANE 95.00%
5MG
$ 495.34

Total 15 raw suppliers

Chemical Property of Hopane Edit

Chemical Property:

Vapor Pressure:4.06E-08mmHg at 25°C
Refractive Index:1.497
Boiling Point:457.4 °C at 760 mmHg
Flash Point:221.8 °C
PSA：0.00000
Density:0.925 g/cm³
LogP:9.13390
Storage Temp.:2-8°C
XLogP3:11.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:1
Exact Mass:412.406901659
Heavy Atom Count:30
Complexity:688

Purity/Quality:

99%, ^*data from raw suppliers

17β(H),21β(H)-Hopane solution 0.1?mg/mL in isooctane, analytical standard ^*data from reagent suppliers

Safty Information:

Pictogram(s): F,Xn,N
Hazard Codes:F,Xn,N
Statements: 11-38-50/53-65-67
Safety Statements: 60-61-62-33-29-16-9

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C
Isomeric SMILES:CC(C)[C@H]1CC[C@]2([C@H]1CC[C@@]3([C@@H]2CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CCCC5(C)C)C)C)C)C

Technology Process of Hopane

There total 22 articles about Hopane 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: 90.0%

: 934356-93-1
1,4-bis-O-benzyl-2,3-O-isopropylidene-5-aldehydo-D-ribitol

: 934356-90-8
30-phenylthiohopane

: C₅₂H₇₈O₅

: 471-62-5,1176-44-9,13849-96-2,33281-23-1,50894-70-7
hopane

Guidance literature:: 30-phenylthiohopane; With 4,4'-di(tert-butyl)-[1,1-biphenyl]yllithium; In tetrahydrofuran;

1,4-bis-O-benzyl-2,3-O-isopropylidene-5-aldehydo-D-ribitol; In tetrahydrofuran; Further stages.;
DOI:10.1002/chem.200600659

Reference yield: 86.0%

: 934356-90-8
30-phenylthiohopane

: 155681-03-1
benzyl 2,3-O-isopropylidene-β-D-ribo-pentodialdo-1,4-furanoside

: C₄₅H₇₀O₅

: 471-62-5,1176-44-9,13849-96-2,33281-23-1,50894-70-7
hopane

Guidance literature:: 30-phenylthiohopane; With 4,4'-di(tert-butyl)-[1,1-biphenyl]yllithium; In tetrahydrofuran;

benzyl 2,3-O-isopropylidene-β-D-ribo-pentodialdo-1,4-furanoside; In tetrahydrofuran; Further stages.;
DOI:10.1002/chem.200600659

Reference yield: 81.0%

: 934356-90-8
30-phenylthiohopane

: 33985-40-9
(3aR,4S,6R,6aR)-tetrahydro-6-methoxy-2,2-dimethylfuro-[3,4-d][1,3]dioxole-4-carbaldehyde

: C₃₉H₆₆O₅

: 471-62-5,1176-44-9,13849-96-2,33281-23-1,50894-70-7
hopane

Guidance literature:: 30-phenylthiohopane; With 4,4'-di(tert-butyl)-[1,1-biphenyl]yllithium; In tetrahydrofuran; at -78 ℃; for 0.05h;

(3aR,4S,6R,6aR)-tetrahydro-6-methoxy-2,2-dimethylfuro-[3,4-d][1,3]dioxole-4-carbaldehyde; In tetrahydrofuran; at 20 ℃; Further stages.;
DOI:10.1002/chem.200600659