BETA-CYCLOCITRAL

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BETA-CYCLOCITRAL

  • Name BETA-CYCLOCITRAL
  • CAS 432-25-7
  • Purity 99%
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Product Details

Buy Good Quality BETA-CYCLOCITRAL 432-25-7 with a minimum purity of 99%

  • Molecular Formula: C10H16 O
  • Molecular Weight: 152.236
  • Vapor Pressure: 0.176mmHg at 25°C 
  • Melting Point: 62-63 C 
  • Refractive Index: n20/D 1.497(lit.) 
  • Boiling Point: 212.1°Cat760mmHg 
  • Flash Point: 76.9°C 
  • PSA: 17.07000 
  • Density: 0.947g/cm3 
  • LogP: 2.71190 

BETA-CYCLOCITRAL(Cas 432-25-7) Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 69, p. 2072, 1947 DOI: 10.1021/ja01200a519Synthesis, p. 781, 1975

Definition

ChEBI: A monoterpenoid formally derived from citral by cyclisation. It is a volatile compound produced by a cyanobacteria.

InChI:InChI=1/C10H16O/c1-8-5-4-6-10(2,3)9(8)7-11/h7H,4-6H2,1-3H3

432-25-7 Relevant articles

Synthesis of chlorins and bacteriochlorins from cycloaddition reactions with porphyrins

Cavaleiro, José A. S.,Monteiro, Carlos J. P.,Moura, Nuno M. M.,P. M. S. Neves, M. Gra?a,Tomé, Augusto C.

, (2022/02/10)

Chlorins and bacteriochlorins are reduce...

An unexpected generation of magnetically separable Se/Fe3O4 for catalytic degradation of polyene contaminants with molecular oxygen

Chen, Xingyu,Mao, Jingfei,Liu, Chuang,Chen, Chao,Cao, Hongen,Yu, Lei

supporting information, p. 3205 - 3208 (2020/08/12)

Selenization of Fe2O3 with NaHSe led to ...

Scalable synthesis of the aroma compounds d6-β-ionone and d6-β-cyclocitral for use as internal standards in stable isotope dilution assays

Mosaferi, Shabnam,Jelley, Rebecca E.,Fedrizzi, Bruno,Barker, David

supporting information, (2020/12/02)

C13 Norisoprenoids are important aroma c...

A Simple, Mild and General Oxidation of Alcohols to Aldehydes or Ketones by SO2F2/K2CO3 Using DMSO as Solvent and Oxidant

Zha, Gao-Feng,Fang, Wan-Yin,Leng, Jing,Qin, Hua-Li

supporting information, p. 2262 - 2267 (2019/04/17)

A practical, general and mild oxidation ...

432-25-7 Process route

beta-carotene
7235-40-7

beta-carotene

(E)-β-ionone
79-77-6,14901-07-6

(E)-β-ionone

4,9,13-trimethyl-15-(2,6,6-trimethylcyclohex-1-enyl)pentadeca-2,4,6,8,10,12,14-heptaenal
640-49-3

4,9,13-trimethyl-15-(2,6,6-trimethylcyclohex-1-enyl)pentadeca-2,4,6,8,10,12,14-heptaenal

2,6,6-trimethylcyclohex-1-enecarbaldehyde
432-25-7

2,6,6-trimethylcyclohex-1-enecarbaldehyde

trans-β-apo-8'-carotenal
1107-26-2,4172-46-7

trans-β-apo-8'-carotenal

5,6-epoxy-trans-β-ionone
36340-49-5

5,6-epoxy-trans-β-ionone

Conditions
Conditions Yield
With tert.-butylhydroperoxide; μ-carbido-bis[(5,10,15,20-tetraphenyl-21H,23H-porphyrinato)iron(IV)]; In benzene; at 24.84 ℃; Reagent/catalyst; Kinetics;
With tert.-butylhydroperoxide; μ-carbido bis(2,3,7,8,12,13,17,18-octapropyl-5,10,15,20-tetraazaporphinato)iron(IV); In benzene; at 25 ℃; Reagent/catalyst; Kinetics;
α-cyclocitral
14505-74-9,41721-03-3,59462-59-8,432-24-6

α-cyclocitral

2,6,6-trimethylcyclohex-1-enecarbaldehyde
432-25-7

2,6,6-trimethylcyclohex-1-enecarbaldehyde

Conditions
Conditions Yield
With phosphoric acid; Kochen des Reaktionsprodukts mit Alkalilauge;

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432-25-7 Downstream products

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    68826-40-4

    (E)-4-methyl-1-(2',6',6'-trimethylcyclohex-1'-en-1'-yl)pent-1-en-3-one

  • 14393-37-4
    14393-37-4

    5,4-Dihydro-4-methyl-6-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2H-pyran-2-one

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    α,2,6,6-tetramethyl-1-cyclohexene-1-methanol

  • 461-11-0
    461-11-0

    geronic acid

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