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Boc-Phe-dl-(4-thiazolyl)alanine 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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  • 108868-87-7 Structure
  • Basic information

    1. Product Name: Boc-Phe-dl-(4-thiazolyl)alanine methyl ester
    2. Synonyms: Boc-Phe-dl-(4-thiazolyl)alanine methyl ester
    3. CAS NO:108868-87-7
    4. Molecular Formula:
    5. Molecular Weight: 433.528
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 108868-87-7.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: Boc-Phe-dl-(4-thiazolyl)alanine methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Boc-Phe-dl-(4-thiazolyl)alanine methyl ester(108868-87-7)
    11. EPA Substance Registry System: Boc-Phe-dl-(4-thiazolyl)alanine methyl ester(108868-87-7)
  • 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: 108868-87-7(Hazardous Substances Data)

108868-87-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108868-87-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,8,6 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 108868-87:
(8*1)+(7*0)+(6*8)+(5*8)+(4*6)+(3*8)+(2*8)+(1*7)=167
167 % 10 = 7
So 108868-87-7 is a valid CAS Registry Number.

108868-87-7Relevant articles and documents

Novel Renin Inhibitors Containing Analogues of Statine Retro-Inverted at the C-Termini: Specificity at the P2 Histidine Site

Rosenberg, Saul H.,Plattner, Jacob J.,Woods, Keith W.,Stein, Herman H.,Marcotte, Patrick A.,et al.

, p. 1224 - 1228 (2007/10/02)

Substituted 1,3- and 1,4-diamines were prepared from epoxides derived from Boc-leucine or Boc-cyclohexylalanine. These diamines were incorporated into renin inhibitors (IC50 = 4-1500 nM) replacing the Leu-Val scissile bond in small peptide analogues of angiotensinogen. Replacement of the P2 histidine imidazole with other heterocycles maintained or enhanced binding while changing the overall basicity of the inhibitor. Finally, substitution of O-methyltyrosine for the P3 phenylalanine suppressed chymotrypsin cleavage of the P3-P2 bond.

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