Cas 437755-23-2,methyl-[4-oxo-2-(pyrimidin-2-ylamino)-1,4,5,6-tetrahydro-pyrimidin-5-yl]-carbamic acid benzyl ester

437755-23-2

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Basic information

Product Name: methyl-[4-oxo-2-(pyrimidin-2-ylamino)-1,4,5,6-tetrahydro-pyrimidin-5-yl]-carbamic acid benzyl ester
Synonyms: methyl-[4-oxo-2-(pyrimidin-2-ylamino)-1,4,5,6-tetrahydro-pyrimidin-5-yl]-carbamic acid benzyl ester
CAS NO:437755-23-2
Molecular Formula:
Molecular Weight: 354.368
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: methyl-[4-oxo-2-(pyrimidin-2-ylamino)-1,4,5,6-tetrahydro-pyrimidin-5-yl]-carbamic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: methyl-[4-oxo-2-(pyrimidin-2-ylamino)-1,4,5,6-tetrahydro-pyrimidin-5-yl]-carbamic acid benzyl ester(437755-23-2)
EPA Substance Registry System: methyl-[4-oxo-2-(pyrimidin-2-ylamino)-1,4,5,6-tetrahydro-pyrimidin-5-yl]-carbamic acid benzyl ester(437755-23-2)

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: 437755-23-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 437755-23-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,7,7,5 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 437755-23:
(8*4)+(7*3)+(6*7)+(5*7)+(4*5)+(3*5)+(2*2)+(1*3)=172
172 % 10 = 2
So 437755-23-2 is a valid CAS Registry Number.

437755-23-2Upstream product

437755-23-2Downstream Products

437755-25-4 ((S)-5-Benzyloxycarbonylamino-6-{methyl-[4-oxo-2-(pyrimidin-2-ylamino)-1,4,5,6-tetrahydro-pyrimidin-5-yl]-carbamoyl}-hexyl)-carbamic acid benzyl ester

437755-23-2Relevant academic research and scientific papers

Pyrimidinone antibiotics - Heterocyclic analogues with improved antibacterial spectrum

Brands, Michael,Grande, Yolanda Cancho,Endermann, Rainer,Gahlmann, Reinhold,Krueger, Jochen,Raddatz, Siegfried

, p. 2641 - 2645 (2003)

We report the synthesis and pharmacological evaluation of new derivatives of the natural dipeptide antibiotic TAN 1057 A,B containing heterocycles either in the β-amino acid side chain or as mimics of the urea function. In the course of this program, we identified novel analogues that display activity towards a broader panel of Gram-positive bacteriae.

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