160219-64-7

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Basic information

Product Name: Glycine,N-[2-(3,5-dichloro-4-hydroxyphenyl)-2-oxoacetyl]-D-alanyl-(2R)-2-(3,5-dichloro-4-hydroxyphenyl)glycyl-(2R)-2-(3,4-dihydroxyphenyl)glycyl-(2R)-2-(3,5-dichloro-4-hydroxyphenyl)glycyl-N-methyl-L-tyrosyl-2-(4-hydroxyphenyl)-,cyclic (33®5)-ether, cyclic13,35-(1H-indole-3,7-diyl) deriv., (2R)-
Synonyms: Benzeneaceticacid, a-[[[3,27-bis(3,5-dichloro-4-hydroxyphenyl)-6-[[(3,5-dichloro-4-hydroxyphenyl)oxoacetyl]amino]-2,3,4,5,6,7,23,24,25,26,27,28,29,29a-tetradecahydro-32-hydroxy-25-methyl-2,5,26,29-tetraoxo-1H-19,22-etheno-8,9,13-(metheniminomethyno)-14,17-metheno[1,7,10]oxadiazacyclohexadecino[5,4-e]-1,4-diazacycloheptadecin-24-yl]carbonyl]amino]-4-hydroxy-,[3R-[3R*,6R*,24S*(R*),27R*,29aR*]]-; Glycine,N-[(3,5-dichloro-4-hydroxyphenyl)oxoacetyl]-D-alanyl-(2R)-2-(3,5-dichloro-4-hydroxyphenyl)glycyl-(2R)-2-(3,4-dihydroxyphenyl)glycyl-(2R)-2-(3,5-dichloro-4-hydroxyphenyl)glycyl-N-methyl-L-tyrosyl-2-(4-hydroxyphenyl)-,cyclic (33®5)-ether, cyclic13,35-(1H-indole-3,7-diyl) deriv., (2R)- (9CI); Chloropeptin; Chloropeptin I;Sch 79236; WK 3419B
CAS NO:160219-64-7
Molecular Formula: C61H45 Cl6 N7 O15
Molecular Weight: 1328.78
EINECS: N/A
Product Categories: N/A
Mol File: 160219-64-7.mol
Article Data: 4

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Glycine,N-[2-(3,5-dichloro-4-hydroxyphenyl)-2-oxoacetyl]-D-alanyl-(2R)-2-(3,5-dichloro-4-hydroxyphenyl)glycyl-(2R)-2-(3,4-dihydroxyphenyl)glycyl-(2R)-2-(3,5-dichloro-4-hydroxyphenyl)glycyl-N-methyl-L-tyrosyl-2-(4-hydroxyphenyl)-,cyclic (33®5)-ether, cyclic13,35-(1H-indole-3,7-diyl) deriv., (2R)-(CAS DataBase Reference)
NIST Chemistry Reference: Glycine,N-[2-(3,5-dichloro-4-hydroxyphenyl)-2-oxoacetyl]-D-alanyl-(2R)-2-(3,5-dichloro-4-hydroxyphenyl)glycyl-(2R)-2-(3,4-dihydroxyphenyl)glycyl-(2R)-2-(3,5-dichloro-4-hydroxyphenyl)glycyl-N-methyl-L-tyrosyl-2-(4-hydroxyphenyl)-,cyclic (33®5)-ether, cyclic13,35-(1H-indole-3,7-diyl) deriv., (2R)-(160219-64-7)
EPA Substance Registry System: Glycine,N-[2-(3,5-dichloro-4-hydroxyphenyl)-2-oxoacetyl]-D-alanyl-(2R)-2-(3,5-dichloro-4-hydroxyphenyl)glycyl-(2R)-2-(3,4-dihydroxyphenyl)glycyl-(2R)-2-(3,5-dichloro-4-hydroxyphenyl)glycyl-N-methyl-L-tyrosyl-2-(4-hydroxyphenyl)-,cyclic (33®5)-ether, cyclic13,35-(1H-indole-3,7-diyl) deriv., (2R)-(160219-64-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 160219-64-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 160219-64-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,2,1 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 160219-64:
(8*1)+(7*6)+(6*0)+(5*2)+(4*1)+(3*9)+(2*6)+(1*4)=107
107 % 10 = 7
So 160219-64-7 is a valid CAS Registry Number.

160219-64-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name	chloropeptin I

1.2 Other means of identification

Product number	-
Other names	CEHD

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:160219-64-7 SDS

160219-64-7Upstream product

160219-64-7Downstream Products

6324-01-2 p-hydroxyphenylglycine

160219-64-7Relevant articles and documents

Complestatin to chloropeptin I via a quantitative acid catalyzed rearrangement. Absolute stereochemical determination of complestatin

Jayasuriya, Hiranthi,Salituro, Gino M.,Smith, Scott K.,Heck, James V.,Gould, Steven J.,Singh, Sheo B.,Homnick, Carl F.,Holloway, M. Katharine,Pitzenberger, Steven M.,Patane, Michael A.

, p. 2247 - 2248 (1998)

Complestatin and isomeric chloropeptin I are bicyclo hexapeptides isolated from a Streptomyces sp. Both of these compounds are inhibitors of gp120-CD4 HIV fusion activity. In this paper, we describe an efficient acid catalyzed conversion of complestatin t

Total synthesis of chloropeptin II (complestatin) and chloropeptin I

Garfunkle, Joie,Kimball, F. Scott,Trzupek, John D.,Takizawa, Shinobu,Shimamura, Hiroyuki,Tomishima, Masaki,Boger, Dale L.

supporting information; experimental part, p. 16036 - 16038 (2010/02/15)

(Chemical Equation Presented) The first total synthesis of chloropeptin II (1, complestatin) is disclosed. Key elements of the approach include the use of an intramolecular Larock indole synthesis for the initial macrocyclization, adopting conditions that

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