65594-96-9 Usage
Structure
Complex compound with a propionic acid backbone, phenyl, and isoindoline ring attachments.
Usage
Chemical intermediate in pharmaceutical and agrochemical synthesis.
Potential Applications
Medicine: Development of new drugs.
Agriculture: Production of pesticides or fertilizers.
Handling Requirements
Careful handling due to its complex structure and potential reactivity.
Thorough understanding of its chemical properties necessary for safe use.
Check Digit Verification of cas no
The CAS Registry Mumber 65594-96-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,5,9 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 65594-96:
(7*6)+(6*5)+(5*5)+(4*9)+(3*4)+(2*9)+(1*6)=169
169 % 10 = 9
So 65594-96-9 is a valid CAS Registry Number.
InChI:InChI=1/C19H15NO6/c1-11(21)26-13-8-6-12(7-9-13)10-16(19(24)25)20-17(22)14-4-2-3-5-15(14)18(20)23/h2-9,16H,10H2,1H3,(H,24,25)/p-1/t16-/m1/s1
65594-96-9Relevant articles and documents
Trifluoroborane-catalyzed C-H functionalization/S-H insertion reaction: Construction of N,S-acetal quaternary centers
Cai, Yan,Ge, Haihong,Sun, Weize,Miao, Zhiwei
supporting information, p. 1669 - 1677 (2015/06/02)
Abstract The trifluoroborane-catalyzed C-H functionalization/S-H insertion reaction of α-diazophosphonates with thiols has been developed. A plausible reaction mechanism has been proposed to understand the combined reaction. This process provides straightforward access to N,S-acetals containing quaternary centers in moderate to good yields and chemoselectivity.
