Cas 1571839-41-2,(9H-fluoren-9-yl)methyl 1-(1-(benzyloxyamino)-1-oxo-3-phenylpropan-2-ylamino)-1-oxopropan-2-ylcarbamate

1571839-41-2

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Basic information

Product Name: (9H-fluoren-9-yl)methyl 1-(1-(benzyloxyamino)-1-oxo-3-phenylpropan-2-ylamino)-1-oxopropan-2-ylcarbamate
Synonyms:
CAS NO:1571839-41-2
Molecular Formula:
Molecular Weight: 563.653
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: (9H-fluoren-9-yl)methyl 1-(1-(benzyloxyamino)-1-oxo-3-phenylpropan-2-ylamino)-1-oxopropan-2-ylcarbamate(CAS DataBase Reference)
NIST Chemistry Reference: (9H-fluoren-9-yl)methyl 1-(1-(benzyloxyamino)-1-oxo-3-phenylpropan-2-ylamino)-1-oxopropan-2-ylcarbamate(1571839-41-2)
EPA Substance Registry System: (9H-fluoren-9-yl)methyl 1-(1-(benzyloxyamino)-1-oxo-3-phenylpropan-2-ylamino)-1-oxopropan-2-ylcarbamate(1571839-41-2)

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: 1571839-41-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1571839-41-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,7,1,8,3 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1571839-41:
(9*1)+(8*5)+(7*7)+(6*1)+(5*8)+(4*3)+(3*9)+(2*4)+(1*1)=192
192 % 10 = 2
So 1571839-41-2 is a valid CAS Registry Number.

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1571839-41-2Relevant academic research and scientific papers

Synthesis of O-benzyl hydroxamates employing the sulfonate esters of N-hydroxybenzotriazole

Palakurthy, Nani Babu,Dev, Dharm,Paikaray, Sonali,Chaudhury, Susmitnarayan,Mandal, Bhubaneswar

, p. 7952 - 7958 (2014/02/14)

The direct conversion of various carboxylic acids, that include sterically hindered amino acids and di-peptides, to O-benzyl hydroxamates is demonstrated using sulfonate esters of benzotriazoles under ambient and milder conditions without significant race

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