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871578-71-1

(R)-(-)-2-benzylamino-4-(5-phenyl-1H-pyrazol-3-yl)butyric acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 871578-71-1 Structure

  • Basic information

    1. Product Name: (R)-(-)-2-benzylamino-4-(5-phenyl-1H-pyrazol-3-yl)butyric acid methyl ester
    2. Synonyms: (R)-(-)-2-benzylamino-4-(5-phenyl-1H-pyrazol-3-yl)butyric acid methyl ester
    3. CAS NO:871578-71-1
    4. Molecular Formula:
    5. Molecular Weight: 349.433
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 871578-71-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (R)-(-)-2-benzylamino-4-(5-phenyl-1H-pyrazol-3-yl)butyric acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-(-)-2-benzylamino-4-(5-phenyl-1H-pyrazol-3-yl)butyric acid methyl ester(871578-71-1)
    11. EPA Substance Registry System: (R)-(-)-2-benzylamino-4-(5-phenyl-1H-pyrazol-3-yl)butyric acid methyl ester(871578-71-1)

  • 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: 871578-71-1(Hazardous Substances Data)

871578-71-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 871578-71-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,5,7 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 871578-71:
(8*8)+(7*7)+(6*1)+(5*5)+(4*7)+(3*8)+(2*7)+(1*1)=211
211 % 10 = 1
So 871578-71-1 is a valid CAS Registry Number.

871578-71-1Downstream Products

871578-71-1Relevant articles and documents

A convenient approach to the synthesis of ω-heterocyclic amino acids from carboxy lactams through ring-chain transformation; part 1: Synthesis of (2S)-/(2R)-2-amino-4-(1-aryl-/1,5-diaryl-1H-pyrazol-3-yl)butyric acid

Singh, Rakesh K.,Sinha, Neelima,Jain, Sanjay,Salman, Mohammad,Naqvi, Fehmida,Anand, Nitya

, p. 2765 - 2771 (2005)

A general method is reported for the synthesis of co-heterocyclic α-amino acids, which involves preparation of enaminone intermediates from thiolactams, followed by reaction with dinucleophiles, resulting in a single-step condensation and ring-chain trans

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