84274-33-9 Usage
Main properties
1. Compound type: 2-Propenamide
2. Functional groups: amide, acetyl, phenyl
3. Molecular structure: propenamide backbone with acetyl and phenyl groups attached
4. Stereochemistry: (S)-stereoisomer
5. Potential applications: pharmaceuticals, materials science
Specific content
1. Compound name: 2-Propenamide, 2-(acetylamino)-3-phenyl-N-[1-[(phenylmethoxy)methyl]-2-phenylethyl]-, (S)-
2. Functional groups present: amide, acetyl, phenyl
3. Molecular structure: propenamide backbone with acetyl and phenyl groups attached
4. Stereoisomer: (S)-designation
5. Potential applications: pharmaceuticals, materials science
6. Caution: acrylamides can be toxic if not handled properly
Check Digit Verification of cas no
The CAS Registry Mumber 84274-33-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,2,7 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 84274-33:
(7*8)+(6*4)+(5*2)+(4*7)+(3*4)+(2*3)+(1*3)=139
139 % 10 = 9
So 84274-33-9 is a valid CAS Registry Number.
84274-33-9Relevant academic research and scientific papers
SYNTHESIS OF CHIRAL OLIGOPEPTIDES BY MEANS OF CATALYTIC ASYMMETRIC HYDROGENATION OF DEHYDROPEPTIDES
Ojima, Iwao,Yoda, Noriko,Yatabe, Momoko,Tanaka, Toshiyuki,Kogure, Tetsuo
, p. 1255 - 1268 (2007/10/02)
Asymmetric hydrogenation of Ac-ΔTyr(Ac)-(S)-Ala-Gly-OMe (6), Ac-ΔTyr(Ac)-(R)-Ala-Gly-(S)-Phe-OMe (7), Ac-ΔPhe-NH-CH(R)-CH2-OCH2Ph (10), HCO-ΔPhe-(S)-Leu-OMe (16), X-AA-ΔPhe-AA'-OMe ( 5: X=tBOC, CBZ, CF3CO; AA, AA'= α-amino acid ), and t
