Welcome to LookChem.com Sign In|Join Free
  • or
(syn)-(+/-)-7-hydroxymethyl-1,7-dimethylbicyclo<2.2.1>heptane-2-one is a complex organic compound with the molecular formula C10H16O2. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it exists as a racemic mixture, containing both the (+) and (-) enantiomers. This bicyclic ketone features a seven-membered ring with two methyl groups at positions 1 and 7, a hydroxymethyl group at position 7, and a ketone functional group at position 2. Due to its unique structure, it has potential applications in the synthesis of various pharmaceuticals and natural products. However, further research is needed to explore its specific properties, reactivity, and potential uses in the chemical industry.

3751-95-9

Post Buying Request

3751-95-9 Suppliers

Recommended suppliers

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

3751-95-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3751-95-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,5 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3751-95:
(6*3)+(5*7)+(4*5)+(3*1)+(2*9)+(1*5)=99
99 % 10 = 9
So 3751-95-9 is a valid CAS Registry Number.

3751-95-9Upstream product

3751-95-9Relevant academic research and scientific papers

Multiple monohydroxylation products from rac-camphor by marine fungus Botryosphaeria sp. Isolated from marine alga Bostrychia radicans

De Jesus, Hugo C.R.,Jeller, Alex H.,Debonsi, Hosana M.,Alves, Péricles B.,Porto, André L.M.

, p. 498 - 504 (2017)

This manuscript describes the biooxidation of rac-camphor using whole cells of marine-derived fungus Botryosphaeria sp. CBMAI 1197. The main biotransformation products of this monoterpene were achieved via a hydroxylation reaction and occurred with 5 days of rac-camphor incubation. Products were identified by means of gas chromatography mass spectrometry (GC-MS) and nuclear magnetic resonance (NMR) data. The major hydroxylated products were 6-endo-hydroxycamphor, 6-exo-hydroxycamphor, 5-exo-hydroxycamphor, 5-endo-hydroxycamphor, 3-exo-hydroxycamphor and 8-hydroxycamphor. The 6-exo-hydroxycamphor was obtained through a retro-aldol reaction when 6-endo-hydroxycamphor was maintained in presence of CDCl3; this isomerization was confirmed by 1H NMR and GC-MS data.

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 3751-95-9