Cas 109880-46-8,(R)-2-((R)-3-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-propionylamino)-5-(4-methoxy-phenyl)-pentanoic acid

109880-46-8

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Basic information

Product Name: (R)-2-((R)-3-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-propionylamino)-5-(4-methoxy-phenyl)-pentanoic acid
Synonyms: (R)-2-((R)-3-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-propionylamino)-5-(4-methoxy-phenyl)-pentanoic acid
CAS NO:109880-46-8
Molecular Formula:
Molecular Weight: 543.617
EINECS: N/A
Product Categories: N/A

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: (R)-2-((R)-3-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-propionylamino)-5-(4-methoxy-phenyl)-pentanoic acid(CAS DataBase Reference)
NIST Chemistry Reference: (R)-2-((R)-3-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-propionylamino)-5-(4-methoxy-phenyl)-pentanoic acid(109880-46-8)
EPA Substance Registry System: (R)-2-((R)-3-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-propionylamino)-5-(4-methoxy-phenyl)-pentanoic acid(109880-46-8)

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: 109880-46-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 109880-46-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,8,8 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 109880-46:
(8*1)+(7*0)+(6*9)+(5*8)+(4*8)+(3*0)+(2*4)+(1*6)=148
148 % 10 = 8
So 109880-46-8 is a valid CAS Registry Number.

109880-46-8Upstream product

78700-06-8 Boc-D-A₂pr(Z)-ONSu

109880-46-8Downstream Products

109880-46-8Relevant academic research and scientific papers

Cyclic Peptides. XXIII. Synthesis of Retro-Enantio-AM-Toxin I

Mihara, Hisakazu,Aoyagi, Haruhiko,Ueno, Tamio,Kato, Tetsuo,Izumiya, Nobuo

, p. 2651 - 2653 (1986)

To characterize a receptive substance in an apple leaf of phytotoxic AM-toxin I, retro-enantiomer of the toxin was synthesized by the solution method.This analog showed no toxic activity, indicating that the specific backbone conformation of the toxin is

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