Cas 1237528-55-0,7,10,10-trimethyl-8-oxo-6,9-dioxa-2,7-diazaundecanoic acid phenylmethyl ester

1237528-55-0

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Basic information

Product Name: 7,10,10-trimethyl-8-oxo-6,9-dioxa-2,7-diazaundecanoic acid phenylmethyl ester
Synonyms: 7,10,10-trimethyl-8-oxo-6,9-dioxa-2,7-diazaundecanoic acid phenylmethyl ester
CAS NO:1237528-55-0
Molecular Formula:
Molecular Weight: 338.404
EINECS: N/A
Product Categories: N/A
Mol File: 1237528-55-0.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: 7,10,10-trimethyl-8-oxo-6,9-dioxa-2,7-diazaundecanoic acid phenylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 7,10,10-trimethyl-8-oxo-6,9-dioxa-2,7-diazaundecanoic acid phenylmethyl ester(1237528-55-0)
EPA Substance Registry System: 7,10,10-trimethyl-8-oxo-6,9-dioxa-2,7-diazaundecanoic acid phenylmethyl ester(1237528-55-0)

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: 1237528-55-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1237528-55-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,7,5,2 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1237528-55:
(9*1)+(8*2)+(7*3)+(6*7)+(5*5)+(4*2)+(3*8)+(2*5)+(1*5)=160
160 % 10 = 0
So 1237528-55-0 is a valid CAS Registry Number.

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1237528-55-0Relevant articles and documents

Synthesis of aminooxy and N-alkylaminooxy amines for use in bioconjugation

Carrasco, Michael R.,Alvarado, Carolina I.,Dashner, Scott T.,Wong, Amanda J.,Wong, Michael A.

supporting information; experimental part, p. 5757 - 5759 (2010/11/04)

Five Boc-protected aminooxy and N-alkylaminooxy amines have been synthesized in 60-95% overall yield using a common synthetic strategy from readily available two- and three-carbon Cbz-protected amino alcohols. The amines can be linked to biomolecules via

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