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33532-44-4,MFCD00853767
Catalog No.:AA007EW2

33532-44-4 | 4-Keto Retinal

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5mg
2 weeks  
$1,837.00   $1,286.00
- +
25mg
2 weeks  
$3,490.00   $2,443.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA007EW2
Chemical Name:
4-Keto Retinal
CAS Number:
33532-44-4
Molecular Formula:
C20H26O2
Molecular Weight:
298.4192
MDL Number:
MFCD00853767
SMILES:
O=C/C=C(/C=C/C=C(/C=C/C1=C(C)C(=O)CCC1(C)C)\C)\C
Properties
Computed Properties
 
Complexity:
593  
Covalently-Bonded Unit Count:
1  
Defined Bond Stereocenter Count:
4  
Heavy Atom Count:
22  
Hydrogen Bond Acceptor Count:
2  
Rotatable Bond Count:
5  
XLogP3:
4.8  

Literature

Title: Metabolism and biological activities of topical 4-oxoretinoids in mouse skin.

Journal: The Journal of investigative dermatology 20080401

Title: Synthesis of ring-oxidized retinoids as substrates of mouse class I alcohol dehydrogenase (ADH1).

Journal: Organic & biomolecular chemistry 20041121

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SDS
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Tags:33532-44-4 Molecular Formula|33532-44-4 MDL|33532-44-4 SMILES|33532-44-4 4-Keto Retinal
Catalog No.: AA007EW2
33532-44-4,MFCD00853767
33532-44-4 | 4-Keto Retinal
Pack Size： 5mg
Purity：
2 weeks
$1,837.00 $1,286.00
Pack Size： 25mg
Purity：
2 weeks
$3,490.00 $2,443.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA007EW2
Chemical Name: 4-Keto Retinal
CAS Number: 33532-44-4
Molecular Formula: C20H26O2
Molecular Weight: 298.4192
MDL Number: MFCD00853767
SMILES: O=C/C=C(/C=C/C=C(/C=C/C1=C(C)C(=O)CCC1(C)C)\C)\C
Properties
Complexity: 593  
Covalently-Bonded Unit Count: 1  
Defined Bond Stereocenter Count: 4  
Heavy Atom Count: 22  
Hydrogen Bond Acceptor Count: 2  
Rotatable Bond Count: 5  
XLogP3: 4.8  
Literature fold

Title: Metabolism and biological activities of topical 4-oxoretinoids in mouse skin.

Journal: The Journal of investigative dermatology20080401

Title: Synthesis of ring-oxidized retinoids as substrates of mouse class I alcohol dehydrogenase (ADH1).

Journal: Organic & biomolecular chemistry20041121

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