Cas 159581-09-6,(S)-2-tert-Butoxycarbonylamino-3-[(E)-(3-phenyl-acryloyl)amino]-propionic acid

159581-09-6

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Basic information

Product Name: (S)-2-tert-Butoxycarbonylamino-3-[(E)-(3-phenyl-acryloyl)amino]-propionic acid
Synonyms: (S)-2-tert-Butoxycarbonylamino-3-[(E)-(3-phenyl-acryloyl)amino]-propionic acid
CAS NO:159581-09-6
Molecular Formula:
Molecular Weight: 334.372
EINECS: N/A
Product Categories: N/A
Mol File: 159581-09-6.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: (S)-2-tert-Butoxycarbonylamino-3-[(E)-(3-phenyl-acryloyl)amino]-propionic acid(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-tert-Butoxycarbonylamino-3-[(E)-(3-phenyl-acryloyl)amino]-propionic acid(159581-09-6)
EPA Substance Registry System: (S)-2-tert-Butoxycarbonylamino-3-[(E)-(3-phenyl-acryloyl)amino]-propionic acid(159581-09-6)

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: 159581-09-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 159581-09-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,5,8 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 159581-09:
(8*1)+(7*5)+(6*9)+(5*5)+(4*8)+(3*1)+(2*0)+(1*9)=166
166 % 10 = 6
So 159581-09-6 is a valid CAS Registry Number.

159581-09-6Upstream product

159581-09-6Downstream Products

159581-09-6Relevant articles and documents

Structural Determinants of Inhibitory Activity of N3-(4-Methoxyfumaroyl)-L-2,3-Diaminopropanoic Acid Towards Glucosamine-6-Phosphate Synthase

Andruszkiewicz, R.,Chmara, H.,Milewski, S.,Kasprzak, L.,Borowski, E.

, p. 673 - 683 (2007/10/02)

A series of N3-acylated L-2,3-diaminopropanoic acid derivatives and analogues have been synthesized and examined for the inhibitory activity towards glucosamine-6-phosphate synthase (E.C. 2.6.1.16) isolated from bacteria and fungi.The results o

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