138625-57-7 Usage
Propenal derivative
It is derived from propenal, which is a three-carbon compound with a carbon-carbon double bond and an aldehyde functional group.
Benzyl group attachment
A benzyl group (C6H5CH2-) is attached to the propenal moiety, which is a phenyl group connected to a methyl group.
Indazole-3-carbonylamino group attachment
An indazole-3-carbonylamino group (a five-membered nitrogen-containing ring with an amide functional group) is also attached to the propenal moiety.
Pharmaceutical industry applications
This compound has potential applications in the development of new drugs due to its unique structure and possible biological activities.
Biological activities and therapeutic properties
The compound may possess biological activities and therapeutic properties that make it valuable for research and development purposes.
Further investigation and study needed
The specific uses and potential effects of 2-(1-benzyloxycarbonyl-1H-indazole-3-carbonylamino)propenal are subject to further investigation and study to determine its full potential.
Check Digit Verification of cas no
The CAS Registry Mumber 138625-57-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,6,2 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 138625-57:
(8*1)+(7*3)+(6*8)+(5*6)+(4*2)+(3*5)+(2*5)+(1*7)=147
147 % 10 = 7
So 138625-57-7 is a valid CAS Registry Number.
138625-57-7Relevant articles and documents
An efficient synthesis of 6-substituted aminohexahydro-1H-1,4-diazepines from 2-substituted aminopropenals
Harada, Hiroshi,Morie, Toshiya,Hirokawa, Yoshimi,Kato, Shiro
, p. 2205 - 2212 (2007/10/03)
Swern oxidation of 2-substituted amino-1,3-propanediols 20a - d, 38, 41, and 42 smoothly proceeded to give the oxidative dehydration products, 2-substituted aminopropenals 17a - d, 43, 45 and 46, respectively. Reaction of the intriguing 2-substituted amin
