Cas 192221-53-7,N-[(S)-Furan-2-yl-((3aR,4R,6R,6aR)-6-methoxy-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-methyl]-N-(4-methoxy-benzyl)-hydroxylamine

192221-53-7

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Basic information

Product Name: N-[(S)-Furan-2-yl-((3aR,4R,6R,6aR)-6-methoxy-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-methyl]-N-(4-methoxy-benzyl)-hydroxylamine
Synonyms: N-[(S)-Furan-2-yl-((3aR,4R,6R,6aR)-6-methoxy-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-methyl]-N-(4-methoxy-benzyl)-hydroxylamine
CAS NO:192221-53-7
Molecular Formula:
Molecular Weight: 405.448
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: N-[(S)-Furan-2-yl-((3aR,4R,6R,6aR)-6-methoxy-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-methyl]-N-(4-methoxy-benzyl)-hydroxylamine(CAS DataBase Reference)
NIST Chemistry Reference: N-[(S)-Furan-2-yl-((3aR,4R,6R,6aR)-6-methoxy-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-methyl]-N-(4-methoxy-benzyl)-hydroxylamine(192221-53-7)
EPA Substance Registry System: N-[(S)-Furan-2-yl-((3aR,4R,6R,6aR)-6-methoxy-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-methyl]-N-(4-methoxy-benzyl)-hydroxylamine(192221-53-7)

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: 192221-53-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 192221-53-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,2,2 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 192221-53:
(8*1)+(7*9)+(6*2)+(5*2)+(4*2)+(3*1)+(2*5)+(1*3)=117
117 % 10 = 7
So 192221-53-7 is a valid CAS Registry Number.

192221-53-7Upstream product

2786-02-9 2-lithiofuran

192221-53-7Downstream Products

192221-53-7Relevant academic research and scientific papers

Applications of Sugar Nitrones in Synthesis: The Total Synthesis of (+)-Polyoxin J

Dondoni, Alessandro,Franco, Santiago,Junquera, Federico,Merchan, Francisco L.,Merino, Pedro,Tejero, Tomas

, p. 5497 - 5507 (1997)

A convergent synthesis of the peptidyl nucleoside antibiotic (inhibitor of chitin biosynthesis) polyoxin J (2) by coupling of 5-O-carbamoyl polyoxamic acid (3) and thymine polyoxin C (4) is described. These compounds were prepared by chain elongation and

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