Home Other Building Blocks 4845-04-9
4845-04-9,MFCD00013777
Catalog No.:AA00DKW3

4845-04-9 | 1-Cyclohexenemethanol

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Purity
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50mg
80%
3 weeks  
$552.00   $387.00
- +
100mg
80%
3 weeks  
$768.00   $538.00
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250mg
80%
3 weeks  
$1,050.00   $735.00
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500mg
80%
3 weeks  
$1,586.00   $1,110.00
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1g
80%
3 weeks  
$2,002.00   $1,402.00
- +
2.5g
80%
3 weeks  
$3,813.00   $2,669.00
- +
5g
80%
3 weeks  
$5,588.00   $3,912.00
- +
10g
80%
3 weeks  
$8,231.00   $5,762.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00DKW3
Chemical Name:
1-Cyclohexenemethanol
CAS Number:
4845-04-9
Molecular Formula:
C38H46O11
Molecular Weight:
678.7652
MDL Number:
MFCD00013777
SMILES:
COC(=O)C1O[C@@H](O[C@H]2CC[C@H]3[C@]2(C)CC[C@@H]2[C@H]3CCc3c2ccc(c3)OCc2ccccc2)C(C([C@H]1OC(=O)C)OC(=O)C)OC(=O)C
NSC Number:
249806
Properties
Computed Properties
 
Complexity:
94.6  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
1.1  

Downstream Synthesis Route

[1]Patent:WO2015/2994,2015,A2.Locationinpatent:Paragraph00237

[2]AngewandteChemie-InternationalEdition,2016,vol.55,p.11198-11202    Angew.Chem.,2016,vol.128,p.11364-11368,5

[3]RecueildesTravauxChimiquesdesPays-Bas,1996,vol.115,p.20-24

[4]TetrahedronLetters,2005,vol.46,p.6101-6104

[5]BioorganicChemistry,2019,vol.89

[6]JournalofHeterocyclicChemistry,1989,vol.26,p.879-881

[7]ChemicalCommunications,2013,vol.49,p.1521-1523

[8]JournaloftheAmericanChemicalSociety,2016,vol.138,p.12073-12076

[9]Patent:CN110357923,2019,A.Locationinpatent:Paragraph0320-0323

[10]AngewandteChemie-InternationalEdition,2016,vol.55,p.11221-11225    Angew.Chem.,2016,vol.128,p.11387-11391,5

[11]JournaloftheAmericanChemicalSociety,2007,vol.129,p.14144-14145

[12]AdvancedSynthesisandCatalysis,2020,vol.362,p.331-336

[13]AngewandteChemie-InternationalEdition,2011,vol.50,p.10421-10424

[14]JournaloftheAmericanChemicalSociety,2014,vol.136,p.7092-7100

[15]JournalofOrganicChemistry,1989,vol.54,p.1789-1792

[16]MedChemComm,2015,vol.6,p.357-362

[17]JournalofOrganicChemistry,1994,vol.59,p.4323-4326

[18]OrganicLetters,2009,vol.11,p.429-432

[19]Patent:WO2017/194663,2017,A1.Locationinpatent:Page/Pagecolumn39;40

[20]AdvancedSynthesisandCatalysis,2018,vol.360,p.1151-1158

[21]BulletindelaSocieteChimiquedeFrance,1948,p.91,92

[22]JournaloftheChemicalSociety.PerkintransactionsI,1972,p.1727-1730

[23]JournaloftheAmericanChemicalSociety,1991,vol.113,p.5093-5095

[24]JournalofOrganicChemistry,1985,vol.50,p.5193-5199

[25]JournalofOrganicChemistry,1998,vol.63,p.3099-3104

[26]Tetrahedron,2001,vol.57,p.7035-7045

[27]OrganicLetters,2002,vol.4,p.3855-3858

[28]Tetrahedron,2004,vol.60,p.7375-7389

[29]JournaloftheAmericanChemicalSociety,2007,vol.129,p.8710-8711

[30]JournalofOrganicChemistry,2008,vol.73,p.741-744

[31]Patent:US6353006,2002,B1.Locationinpatent:Pagecolumn32-33

[32]ChemicalCommunications,2011,vol.47,p.7857-7859

[33]Chemistry-AEuropeanJournal,2014,vol.20,p.12740-12744

[34]ChemicalCommunications,2016,vol.52,p.8313-8316

[35]OrganicLetters,2017,vol.19,p.3703-3706

[36]AngewandteChemie-InternationalEdition,2018,vol.57,p.16857-16860    Angew.Chem.,2018,vol.130,p.17099-17102,4

[37]AngewandteChemie-InternationalEdition,2019,vol.58,p.4700-4704    Angew.Chem.,2019,vol.131,p.4748-4752,5

[38]AdvancedSynthesisandCatalysis,2019,vol.361,p.4919-4925

4845-04-9   
platinum 
  100-49-2 

[1]JournaloftheAmericanChemicalSociety,1939,vol.61,p.1057,1059

[1]JournalofCatalysis,2007,vol.250,p.33-40

4845-04-9    116119-01-8   
methyl7-(cyclohex-1-en-1-ylmethoxy)benzod1,3dioxole-5-carboxylate 

[1]AdvancedSynthesisandCatalysis,2015,vol.357,p.3880-3884

4845-04-9    73505-48-3   
methyl3-(cyclohex-1-en-1-ylmethoxy)-4-methylbenzoate 

[1]AdvancedSynthesisandCatalysis,2015,vol.357,p.3880-3884

Literature

Title: Generating a generation of proteasome inhibitors: from microbial fermentation to total synthesis of salinosporamide a (marizomib) and other salinosporamides.

Journal: Marine drugs 20100101

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