Welcome to LookChem.com Sign In|Join Free
  • or
(3S*,4R*)-4-hydroxy-3-methylpentene is a chiral organic compound characterized by its unique stereochemistry. It features a hydroxyl group (-OH) at the 4th carbon and a methyl group (-CH3) at the 3rd carbon, with the double bond positioned between the 3rd and 4th carbons. The compound's stereochemistry is defined by the R and S configurations at the 3rd and 4th carbons, respectively, indicating the spatial arrangement of the substituents around the chiral centers. This specific arrangement is crucial for its chemical properties and potential applications in various fields, such as pharmaceuticals or chemical synthesis, where stereochemistry plays a significant role in determining the compound's activity and reactivity.

1538-22-3

Post Buying Request

1538-22-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1538-22-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1538-22-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,3 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1538-22:
(6*1)+(5*5)+(4*3)+(3*8)+(2*2)+(1*2)=73
73 % 10 = 3
So 1538-22-3 is a valid CAS Registry Number.

1538-22-3Downstream Products

1538-22-3Relevant academic research and scientific papers

Allylstannation X. Stereochemical course of the Addition Reactions of (E/Z)-Bu3SnCH2CH=CHCH3 with Aldehydes in the Presence of Lewis Acids (Bu2SnCl2, BF3.Et2O, and TiCl4)

Boaretto, Andrea,Marton, Daniele,Tagliavini, Giuseppe,Ganis, Paolo

, p. 199 - 208 (2007/10/02)

Reactions between (E/Z)-Bu3SnCH2CH=CHCH3 and RCHO (R= CH3, C2H5, n-C3H7, n-C4H9, n-C5H11, (CH3)2CH, (CH3)3C, C6H5, CH2=CH, CH2=C(CH3), (E)-CH3CH=CH, (E)-C3H7CH=CH, (E)-C6H5CH=CH) have been carried out in the presence of Lewis acids such as Bu2SnCl2, BF3.Et2O, and TiCl4.The stereochemical course of the reactions to give homoallylic alcohols does not necessarily depend on the formation of intermediate Lewis acid-aldehyde complexes, but rather upon the formation of allylmetal compounds (e.g.Bu2ClSnCH2CH=CHCH3, Bu2ClSnCH(CH3)CH=CHCH2, Cl3TiCH2CH=CHCH3, etc.) which are the actual species which react with the carbonyl compounds.Bu3SnCH2CH=CHCH3 does not undergo the reaction.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1538-22-3