197778-15-7

• 

• Basic information

  1. Product Name: Cyclopropanecarboxylic acid, 1-amino-2-phenyl-, methyl ester, (1R,2S)-rel-
  2. Synonyms: Cyclopropanecarboxylic acid, 1-amino-2-phenyl-, methyl ester, (1R,2S)-rel-;methyl (1S,2R)-1-amino-2-phenyl-cyclopropanecarboxylate
  3. CAS NO:197778-15-7
  4. Molecular Formula: C11H13NO2
  5. Molecular Weight: 191.22642
  6. EINECS: N/A
  7. Product Categories: AMINOACID
  8. Mol File: 197778-15-7.mol
  9. Article Data: 10

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: Cyclopropanecarboxylic acid, 1-amino-2-phenyl-, methyl ester, (1R,2S)-rel-(CAS DataBase Reference)
  10. NIST Chemistry Reference: Cyclopropanecarboxylic acid, 1-amino-2-phenyl-, methyl ester, (1R,2S)-rel-(197778-15-7)
  11. EPA Substance Registry System: Cyclopropanecarboxylic acid, 1-amino-2-phenyl-, methyl ester, (1R,2S)-rel-(197778-15-7)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 197778-15-7(Hazardous Substances Data)

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197778-15-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 197778-15-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,7,7,7 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 197778-15:
(8*1)+(7*9)+(6*7)+(5*7)+(4*7)+(3*8)+(2*1)+(1*5)=207
207 % 10 = 7
So 197778-15-7 is a valid CAS Registry Number.

197778-15-7Upstream product

• 100-42-5 styrene 
• 2483-57-0 methyl 2-nitroacetate 
• 15431-30-8 methyl 2-diazo-2-nitroacetate 
• 82112-04-7 methyl (E)-2-phenyl-1-aminocyclopropane-1-carboxylate hydrochloride 
• 1095278-82-2 methyl (1S,2S)-1-nitro-2-phenylcyclopropanecarboxylate 
• 1036637-32-7 methyl (1S,2R)-1-nitro-2-phenylcyclopropanecarboxylate 
• 110769-85-2 C₁₁H₁₃NO₂*C₁₈H₁₄O₈ 
• 100-52-7 benzaldehyde 
• 82112-04-7 Cyclopropyl-Z-phenylalanine methyl ester hydrochloride 
• 3092-20-4 diethyl 2-phenylcyclopropane-1,1-dicarboxylate 
• 5292-53-5 diethyl benzalmalonate 
• 70315-54-7 methyl 1-benzamido-2-phenyl-cyclopropanecarboxylate 
• 180322-84-3 monomethyl (1S,2R)-2-phenylcyclopropane-1,1-dicarboxylate 
• 123806-61-1 C₁₉H₁₉NO₄ 

197778-15-7Downstream Products

• 150408-99-4 (1S,2R)-1-[(R)-2-(Adamantan-2-yloxycarbonylamino)-3-(1H-indol-3-yl)-2-methyl-propionylamino]-2-phenyl-cyclopropanecarboxylic acid methyl ester 
• 150351-75-0 (1S,2S)-1-[(R)-2-(Adamantan-2-yloxycarbonylamino)-3-(1H-indol-3-yl)-2-methyl-propionylamino]-2-phenyl-cyclopropanecarboxylic acid methyl ester 
• 197778-21-5 (S)-2-((1R,2S)-1-Methylcarbamoyl-2-phenyl-cyclopropylcarbamoyl)-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 197778-22-6 (S)-2-((1S,2R)-1-Methylcarbamoyl-2-phenyl-cyclopropylcarbamoyl)-pyrrolidine-1-carboxylic acid tert-butyl ester 

197778-15-7Relevant articles and documents

A formyl peptide substituted with a conformationally constrained phenylalanine residue evokes a selective immune response in human neutrophils

Hayashi, Ryo,Miyazaki, Masaya,Osada, Satoshi,Kawasaki, Hiroshi,Fujita, Ichiro,Hamasaki, Yuhei,Kodama, Hiroaki

supporting information, p. 668 - 675 (2013/02/25)

Formyl-Met-Leu-Phe-OH (fMLP) binds to formyl peptide receptors, FPR1 and FPR2, and evokes migration and superoxide anion production in human neutrophils. To obtain a more effective and selective ligand, fMLP analogs in which the Phe residue was substitute

CATHEPSIN CYSTEINE PROTEASE INHIBITORS FOR THE TREATMENT OF VARIOUS DISEASES

-

Page/Page column 32-33, (2011/01/12)

The present invention relates to compounds capable of inhibiting and/or decreasing the activity of one or more cathepsins, thereby treating and/or preventing various disease states associated with one or more cysteine proteases including, but not limited

PEPTIDYL NITRILES AND USE THEREOF AS DIPEPTIDYL PEPTIDASE I INHIBITORS

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Page/Page column 62, (2009/07/17)

The present invention provides compounds of formula (I) in which n, y, X1, X2, A, B, R1, R2, R3, R4 and R5 are as defined in the specification, a process for their preparation, pharmaceutical compositions containing them and their use as dipeptidyl peptidase I (DPPI) inhibitors.

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