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2-{(S)-1-[(2-{[(R)-1-((2S,3S)-2-tert-butoxycarbonylamino-3-methylpentanoylamino)-2-methylpropylamino]methyl}[2,4';2',4]teroxazole-4-carbothioyl)amino]-2-hydroxyethyl}-5-phenyloxazole-4-carboxylic 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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  • 2-{(S)-1-[(2-{[(R)-1-((2S,3S)-2-tert-butoxycarbonylamino-3-methylpentanoylamino)-2-methylpropylamino]methyl}[2,4';2',4]teroxazole-4-carbothioyl)amino]-2-hydroxyethyl}-5-phenyloxazole-4-carboxylic acid methyl ester

    Cas No: 860791-85-1

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  • 2-{(S)-1-[(2-{[(R)-1-((2S,3S)-2-tert-butoxycarbonylamino-3-methylpentanoylamino)-2-methylpropylamino]methyl}[2,4';2',4]teroxazole-4-carbothioyl)amino]-2-hydroxyethyl}-5-phenyloxazole-4-carboxylic acid methyl ester

    Cas No: 860791-85-1

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  • 860791-85-1 Structure
  • Basic information

    1. Product Name: 2-{(S)-1-[(2-{[(R)-1-((2S,3S)-2-tert-butoxycarbonylamino-3-methylpentanoylamino)-2-methylpropylamino]methyl}[2,4';2',4]teroxazole-4-carbothioyl)amino]-2-hydroxyethyl}-5-phenyloxazole-4-carboxylic acid methyl ester
    2. Synonyms: 2-{(S)-1-[(2-{[(R)-1-((2S,3S)-2-tert-butoxycarbonylamino-3-methylpentanoylamino)-2-methylpropylamino]methyl}[2,4';2',4]teroxazole-4-carbothioyl)amino]-2-hydroxyethyl}-5-phenyloxazole-4-carboxylic acid methyl ester
    3. CAS NO:860791-85-1
    4. Molecular Formula:
    5. Molecular Weight: 848.934
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 860791-85-1.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: 2-{(S)-1-[(2-{[(R)-1-((2S,3S)-2-tert-butoxycarbonylamino-3-methylpentanoylamino)-2-methylpropylamino]methyl}[2,4';2',4]teroxazole-4-carbothioyl)amino]-2-hydroxyethyl}-5-phenyloxazole-4-carboxylic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-{(S)-1-[(2-{[(R)-1-((2S,3S)-2-tert-butoxycarbonylamino-3-methylpentanoylamino)-2-methylpropylamino]methyl}[2,4';2',4]teroxazole-4-carbothioyl)amino]-2-hydroxyethyl}-5-phenyloxazole-4-carboxylic acid methyl ester(860791-85-1)
    11. EPA Substance Registry System: 2-{(S)-1-[(2-{[(R)-1-((2S,3S)-2-tert-butoxycarbonylamino-3-methylpentanoylamino)-2-methylpropylamino]methyl}[2,4';2',4]teroxazole-4-carbothioyl)amino]-2-hydroxyethyl}-5-phenyloxazole-4-carboxylic acid methyl ester(860791-85-1)
  • 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: 860791-85-1(Hazardous Substances Data)

860791-85-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 860791-85-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,0,7,9 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 860791-85:
(8*8)+(7*6)+(6*0)+(5*7)+(4*9)+(3*1)+(2*8)+(1*5)=201
201 % 10 = 1
So 860791-85-1 is a valid CAS Registry Number.

860791-85-1Relevant articles and documents

Novel polyoxazole-based cyclopeptides from Streptomyces sp. Total synthesis of the cyclopeptide YM-216391 and synthetic studies towards telomestatin

Deeley, Jon,Bertram, Anna,Pattenden, Gerald

experimental part, p. 1994 - 2010 (2009/01/31)

A convergent, complementary, synthetic approach to the contiguously linked tris-oxazole units 10, 11 and 12 in telomestatin (1) and YM-216391 (2) is described. The route involves coupling reactions between oxazole 4-carboxylic acids, viz16a, 16c, 16d and

Synthesis and establishment of stereochemistry of the unusual polyoxazole-thiazole based cyclopeptide YM-216391 isolated from Streptomyces nobilis

Deeley, Jon,Pattenden, Gerald

, p. 797 - 799 (2007/10/03)

A concise total synthesis of the unusual oxazole-based cyclopeptide structure YM-216391, which also establishes the stereochemistry of the natural product i.e. 1, is described. The Royal Society of Chemistry 2005.

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