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97654-03-0

Mal-Pab-Tyr-OMe is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 97654-03-0 Structure

  • Basic information

    1. Product Name: Mal-Pab-Tyr-OMe
    2. Synonyms:
    3. CAS NO:97654-03-0
    4. Molecular Formula:
    5. Molecular Weight: 394.384
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 97654-03-0.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: Mal-Pab-Tyr-OMe(CAS DataBase Reference)
    10. NIST Chemistry Reference: Mal-Pab-Tyr-OMe(97654-03-0)
    11. EPA Substance Registry System: Mal-Pab-Tyr-OMe(97654-03-0)

  • 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: 97654-03-0(Hazardous Substances Data)

97654-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97654-03-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,6,5 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 97654-03:
(7*9)+(6*7)+(5*6)+(4*5)+(3*4)+(2*0)+(1*3)=170
170 % 10 = 0
So 97654-03-0 is a valid CAS Registry Number.

97654-03-0Downstream Products

97654-03-0Relevant articles and documents

Synthesis of N-Maleoyl-aminoacids and -peptides

Augustin, Manfred,Mueller, Wolfgang

, p. 789 - 798 (2007/10/02)

N-Maleoyl-aminoacid-N'-hydroxysuccinimidesters 3 or N-maleoyl-aminobenzoic acids 5 are synthsized from N-maleyl-aminoacids 1 on different ways.N-maleoyl-aminobenzoic-4-nirophenyl-, -2-nitro-phenyl- or 2,4-dinitro-phenylesters 6, 7 and 8 will be obtained from 1 or 5. o-Mercaptoaniline, thiourea or cysteine react with 5 to benzothiazines 9, thiazolidines 10 and 1,4-thiazines 11.From 5 the peptides 12 are yielded.The pentapeptide 13 are formed from 12 by addition of glutathione.

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