Cas 226895-30-3,(Z)-2-Benzyloxycarbonylamino-oct-2-enoic acid methyl ester

226895-30-3

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Basic information

Product Name: (Z)-2-Benzyloxycarbonylamino-oct-2-enoic acid methyl ester
Synonyms: (Z)-2-Benzyloxycarbonylamino-oct-2-enoic acid methyl ester
CAS NO:226895-30-3
Molecular Formula:
Molecular Weight: 305.374
EINECS: N/A
Product Categories: N/A
Mol File: 226895-30-3.mol
Article Data: 1

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: (Z)-2-Benzyloxycarbonylamino-oct-2-enoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-2-Benzyloxycarbonylamino-oct-2-enoic acid methyl ester(226895-30-3)
EPA Substance Registry System: (Z)-2-Benzyloxycarbonylamino-oct-2-enoic acid methyl ester(226895-30-3)

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: 226895-30-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 226895-30-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,6,8,9 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 226895-30:
(8*2)+(7*2)+(6*6)+(5*8)+(4*9)+(3*5)+(2*3)+(1*0)=163
163 % 10 = 3
So 226895-30-3 is a valid CAS Registry Number.

226895-30-3Upstream product

226895-30-3Downstream Products

101650-10-6 (S)-methyl-(N-benzyloxycarboxyl)-2-aminocaprylate

226895-30-3Relevant articles and documents

Synthesis of enantiomerically pure backbone alkyl substituted peptide nucleic acids utilizing the Et-DuPHOS-Rh+ hydrogenation of enamido esters

Stammers, Timothy A.,Burk, Mark J.

, p. 3325 - 3328 (1999)

A series of enantiomerically pure alkyl substituted peptide nucleic acid (PNA) monomers were synthesized by incorporating novel α-amino acids produced by the Et-DuPHOS-Rh+ catalytic asymmetric hydrogenation of enamido esters.

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