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370867-67-7

phosphoric acid dibenzyl ester 2-[2,15-dibenzyl-8-sec-butyl-21-hydroxy-5-(4-hydroxy-benzyl)-4,11-dimethyl-3,6,9,13,16,22-hexaoxo-10-oxa-1,4,7,14,17-pentaaza-bicyclo[16.3.1]docos-12-ylcarbamoyl]-2-hydroxy-ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • phosphoric acid dibenzyl ester 2-[2,15-dibenzyl-8-sec-butyl-21-hydroxy-5-(4-hydroxy-benzyl)-4,11-dimethyl-3,6,9,13,16,22-hexaoxo-10-oxa-1,4,7,14,17-pentaaza-bicyclo[16.3.1]docos-12-ylcarbamoyl]-2-hydroxy-ethyl ester

    Cas No: 370867-67-7

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  • 370867-67-7 Structure

  • Basic information

    1. Product Name: phosphoric acid dibenzyl ester 2-[2,15-dibenzyl-8-sec-butyl-21-hydroxy-5-(4-hydroxy-benzyl)-4,11-dimethyl-3,6,9,13,16,22-hexaoxo-10-oxa-1,4,7,14,17-pentaaza-bicyclo[16.3.1]docos-12-ylcarbamoyl]-2-hydroxy-ethyl ester
    2. Synonyms: phosphoric acid dibenzyl ester 2-[2,15-dibenzyl-8-sec-butyl-21-hydroxy-5-(4-hydroxy-benzyl)-4,11-dimethyl-3,6,9,13,16,22-hexaoxo-10-oxa-1,4,7,14,17-pentaaza-bicyclo[16.3.1]docos-12-ylcarbamoyl]-2-hydroxy-ethyl ester
    3. CAS NO:370867-67-7
    4. Molecular Formula:
    5. Molecular Weight: 1147.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 370867-67-7.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: phosphoric acid dibenzyl ester 2-[2,15-dibenzyl-8-sec-butyl-21-hydroxy-5-(4-hydroxy-benzyl)-4,11-dimethyl-3,6,9,13,16,22-hexaoxo-10-oxa-1,4,7,14,17-pentaaza-bicyclo[16.3.1]docos-12-ylcarbamoyl]-2-hydroxy-ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: phosphoric acid dibenzyl ester 2-[2,15-dibenzyl-8-sec-butyl-21-hydroxy-5-(4-hydroxy-benzyl)-4,11-dimethyl-3,6,9,13,16,22-hexaoxo-10-oxa-1,4,7,14,17-pentaaza-bicyclo[16.3.1]docos-12-ylcarbamoyl]-2-hydroxy-ethyl ester(370867-67-7)
    11. EPA Substance Registry System: phosphoric acid dibenzyl ester 2-[2,15-dibenzyl-8-sec-butyl-21-hydroxy-5-(4-hydroxy-benzyl)-4,11-dimethyl-3,6,9,13,16,22-hexaoxo-10-oxa-1,4,7,14,17-pentaaza-bicyclo[16.3.1]docos-12-ylcarbamoyl]-2-hydroxy-ethyl ester(370867-67-7)

  • 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: 370867-67-7(Hazardous Substances Data)

370867-67-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 370867-67-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,0,8,6 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 370867-67:
(8*3)+(7*7)+(6*0)+(5*8)+(4*6)+(3*7)+(2*6)+(1*7)=177
177 % 10 = 7
So 370867-67-7 is a valid CAS Registry Number.

370867-67-7Upstream product

370867-67-7Downstream Products

370867-67-7Relevant articles and documents

Synthetic studies of the cyclic depsipeptides bearing the 3-amino-6-hydroxy-2-piperidone (Ahp) unit. Total synthesis of the proposed structure of micropeptin T-20

Yokokawa, Fumiaki,Inaizumi, Akiko,Shioiri, Takayuki

, p. 1459 - 1480 (2005)

The first total synthesis of a cyclic depsipeptide possessing the 3-amino-6-hydroxy-2-piperidone (Ahp) unit was successfully achieved in a convergent manner by the oxidative construction of the Ahp unit at the later stage of the synthesis. This synthetic work provides data indicating that the structure of the target Ahp-depsipeptide, micropeptin T-20, should be re-examined.

Synthetic studies of micropeptin T-20, a novel 3-amino-6-hydroxy-2-piperidone (Ahp)-containing cyclic depsipeptide

Yokokawa, Fumiaki,Inaizumi, Akiko,Shioiri, Takayuki

, p. 5903 - 5908 (2007/10/03)

The synthetic studies of micropeptin T-20 including the late installation of the Ahp (3-amino-6-hydroxy-2-piperidone) residue through oxidation and cyclization of a homoserine to the requisite hemiaminal are described.

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