Cas 78464-33-2,(E)-2-(2-Benzyloxycarbonylamino-3-hydroxy-butyrylamino)-pent-2-enoic acid ethyl ester

78464-33-2

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Basic information

Product Name: (E)-2-(2-Benzyloxycarbonylamino-3-hydroxy-butyrylamino)-pent-2-enoic acid ethyl ester
Synonyms: (E)-2-(2-Benzyloxycarbonylamino-3-hydroxy-butyrylamino)-pent-2-enoic acid ethyl ester
CAS NO:78464-33-2
Molecular Formula:
Molecular Weight: 378.425
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: (E)-2-(2-Benzyloxycarbonylamino-3-hydroxy-butyrylamino)-pent-2-enoic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (E)-2-(2-Benzyloxycarbonylamino-3-hydroxy-butyrylamino)-pent-2-enoic acid ethyl ester(78464-33-2)
EPA Substance Registry System: (E)-2-(2-Benzyloxycarbonylamino-3-hydroxy-butyrylamino)-pent-2-enoic acid ethyl ester(78464-33-2)

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: 78464-33-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 78464-33-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,4,6 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 78464-33:
(7*7)+(6*8)+(5*4)+(4*6)+(3*4)+(2*3)+(1*3)=162
162 % 10 = 2
So 78464-33-2 is a valid CAS Registry Number.

78464-33-2Upstream product

78464-33-2Downstream Products

78464-39-8 (E)-2-(2-Benzyloxycarbonylamino-3-methanesulfonyloxy-butyrylamino)-pent-2-enoic acid ethyl ester

78464-33-2Relevant academic research and scientific papers

Dehydrooligopeptides. II. The Synthesis of Dehydrodehydrodipeptides by Direct Coupling and Base-catalyzed β-Elimination

Shin, Chung-gi,Yonezawa, Yasuchika,Takahashi, Masatoshi,Yoshimura, Juji

, p. 1132 - 1136 (1981)

The direct coupling between N-protected α-dehydroamino acid (1) and N-free α-dehydroamino acid ester (2) by the acid-chloride method was carried out to give several dehydrodehydrodipeptides (7).Furthermore, the two kinds of dehydrodipeptides with a hydrox

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