46236-19-5 Usage
Type of compound
Methyl ester derivative
Parent compound
1,2-Dithiolane-3-pentanoic acid
Sulfur content
Contains sulfur
Industries
Used in pharmaceutical and agricultural industries
Application
Serves as an intermediate for the synthesis of various pharmaceuticals and agrochemicals
Usage
Used as a fragrance ingredient in perfumes and personal care products
Characteristic
Unique odor
Utilization
Often utilized for its pleasant scent
Potential applications
Organic synthesis due to its reactivity and functional groups
Check Digit Verification of cas no
The CAS Registry Mumber 46236-19-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,6,2,3 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 46236-19:
(7*4)+(6*6)+(5*2)+(4*3)+(3*6)+(2*1)+(1*9)=115
115 % 10 = 5
So 46236-19-5 is a valid CAS Registry Number.
46236-19-5Relevant articles and documents
α-Keto Acid Dehydrogenases: A Chemical Model
Rastetter, William H.,Adams, Julian
, p. 1882 - 1887 (2007/10/02)
A model system for the involvement of lipoic acid in α-keto acid dehydrogenase systems is described. 2-(α-Hydroxyethyl)-3-benzyl-4-methylthiazolium tetrafluoroborate (6) serves as precursor for an analogue of the thiamine-bound active aldehyde 1 in the natural system.The model active aldehyde 7 reacts with linear disulfides, yielding thiols and thioesters.The 1,2-dithiolane, methyl lipoate (14), is unreactive under model reaction conditions.The tetrahedral intermediate which would be formed from methyl lipoate (14) plus an active aldehyde analogue 19 has been generated in a nonbiomimetic fashion.The synthetic tetrahedral intermediate 17 undergoes the reverse of the biological, disulfide reductive cleavage reaction.
