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CAS

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945410-46-8

(3S)-4-bromo-3,5-dimethyl-1-(3-benzyloxyaminobutanoyl)pyrazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 945410-46-8 Structure

  • Basic information

    1. Product Name: (3S)-4-bromo-3,5-dimethyl-1-(3-benzyloxyaminobutanoyl)pyrazole
    2. Synonyms: (3S)-4-bromo-3,5-dimethyl-1-(3-benzyloxyaminobutanoyl)pyrazole
    3. CAS NO:945410-46-8
    4. Molecular Formula:
    5. Molecular Weight: 366.258
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 945410-46-8.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: (3S)-4-bromo-3,5-dimethyl-1-(3-benzyloxyaminobutanoyl)pyrazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3S)-4-bromo-3,5-dimethyl-1-(3-benzyloxyaminobutanoyl)pyrazole(945410-46-8)
    11. EPA Substance Registry System: (3S)-4-bromo-3,5-dimethyl-1-(3-benzyloxyaminobutanoyl)pyrazole(945410-46-8)

  • 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: 945410-46-8(Hazardous Substances Data)

945410-46-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 945410-46-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,5,4,1 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 945410-46:
(8*9)+(7*4)+(6*5)+(5*4)+(4*1)+(3*0)+(2*4)+(1*6)=168
168 % 10 = 8
So 945410-46-8 is a valid CAS Registry Number.

945410-46-8Downstream Products

945410-46-8Relevant articles and documents

Organocatalysis in conjugate amine additions. Synthesis of β-amino acid derivatives

Sibi, Mukund P.,Itoh, Kennosuke

, p. 8064 - 8065 (2008/02/09)

Conjugate addition of O-protected hydroxylamines to pyrazole-derived enoates proceeds with high efficiency and enantioselectivity when chiral thioureas are used as activators. A wide variety of substrates undergo conjugate amine addition providing access to enantioenriched β-amino acid derivatives. Structural requirements for the optimal thiourea catalyst have been established, and the results suggest that it operates as a bifunctional catalyst. Copyright

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