Cas 1031845-64-3,(S)-3-Benzyloxycarbonylamino-N-[(S)-2-(3-hydroxy-phenyl)-1-methoxycarbonyl-ethyl]-succinamic acid benzyl ester

1031845-64-3

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Basic information

Product Name: (S)-3-Benzyloxycarbonylamino-N-[(S)-2-(3-hydroxy-phenyl)-1-methoxycarbonyl-ethyl]-succinamic acid benzyl ester
Synonyms: (S)-3-Benzyloxycarbonylamino-N-[(S)-2-(3-hydroxy-phenyl)-1-methoxycarbonyl-ethyl]-succinamic acid benzyl ester
CAS NO:1031845-64-3
Molecular Formula:
Molecular Weight: 534.566
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: (S)-3-Benzyloxycarbonylamino-N-[(S)-2-(3-hydroxy-phenyl)-1-methoxycarbonyl-ethyl]-succinamic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-3-Benzyloxycarbonylamino-N-[(S)-2-(3-hydroxy-phenyl)-1-methoxycarbonyl-ethyl]-succinamic acid benzyl ester(1031845-64-3)
EPA Substance Registry System: (S)-3-Benzyloxycarbonylamino-N-[(S)-2-(3-hydroxy-phenyl)-1-methoxycarbonyl-ethyl]-succinamic acid benzyl ester(1031845-64-3)

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: 1031845-64-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1031845-64-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,1,8,4 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1031845-64:
(9*1)+(8*0)+(7*3)+(6*1)+(5*8)+(4*4)+(3*5)+(2*6)+(1*4)=123
123 % 10 = 3
So 1031845-64-3 is a valid CAS Registry Number.

1031845-64-3Upstream product

1031845-64-3Downstream Products

72683-64-8 L-aspartyl-L-m-hydroxyphenylalanine methyl ester

1031845-64-3Relevant academic research and scientific papers

Peptide sweeteners. 4. Hydroxy and methoxy substitution of the aromatic ring in L-aspartyl-L-phenylalanine methyl ester. Structure-taste relationships.

Kawai,Chorev,Marin-Rose,Goodman

, p. 420 - 424 (2007/10/02)

A series of analogues of the dipeptide sweetener L-aspartyl-L-phenylalanine methyl ester having hydroxy and/or methoxy substitution on the aromatic ring was synthesized and tasted. The introduction of a methoxy group in the para position of the aromatic r

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