30742-60-0 Usage
General Description
5-Nitro-2-Piperidinobenzaldehyde is a chemical compound that falls under the category of organic compounds. More specifically, it is a benzaldehyde, which means its structure contains a benzene ring with a formyl substituent. This specific benzaldehyde has additional nitro and piperidino group attached, hence the name 5-Nitro-2-Piperidinobenzaldehyde. Benzaldehydes are typically used in the creation of various perfumes and flavorings and they also occur in many essential oils. However, there is no detailed information available on the exact use, properties or safety measures related to this specific compound, hence it is generally suggested to handle it with appropriate care until detailed specifications are known.
Check Digit Verification of cas no
The CAS Registry Mumber 30742-60-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,7,4 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 30742-60:
(7*3)+(6*0)+(5*7)+(4*4)+(3*2)+(2*6)+(1*0)=90
90 % 10 = 0
So 30742-60-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H14N2O3/c15-9-10-8-11(14(16)17)4-5-12(10)13-6-2-1-3-7-13/h4-5,8-9H,1-3,6-7H2
30742-60-0Relevant articles and documents
Construction of the tetrahydroquinoline spiro skeleton: Via cascade [1,5]-hydride transfer-involved C(sp3)-H functionalization "on water"
Zhu, Shuai,Chen, Chunqi,Xiao, Mingyan,Yu, Liping,Wang, Liang,Xiao, Jian
supporting information, p. 5653 - 5658 (2017/12/06)
The pharmaceutically important tetrahydroquinoline spiro compounds were efficiently constructed via cascade SNAr/Knoevenagel condensation/[1,5]-hydride transfer/cyclization on water, featuring high atom-economy and step-economy. This water-base
Protecting-group-free amination of halogenated nitrobenzaldehyde with palladium catalyst
Cao, Jing,Feng, Jun Xiang,Wu, Yong Xiang,Tuo, Ya Ya
experimental part, p. 935 - 938 (2011/11/13)
"One-step" method for the synthesis of secondary aliphatic amine substituted nitrobenzaldehyde was developed. In the presence of Pd catalyst, halogenated nitrobenzaldehyde could be smoothly coupled with secondary aliphatic amine to give the target product
