Cas 883559-62-4,tert-butyl (1R,2Z,6R,7R,9R)-(10-benzyloxy-6-hydroxy-7,9-dimethyl-8-oxo-1-propyl-dec-2-enyl)-carbamate

883559-62-4

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Basic information

Product Name: tert-butyl (1R,2Z,6R,7R,9R)-(10-benzyloxy-6-hydroxy-7,9-dimethyl-8-oxo-1-propyl-dec-2-enyl)-carbamate
Synonyms: tert-butyl (1R,2Z,6R,7R,9R)-(10-benzyloxy-6-hydroxy-7,9-dimethyl-8-oxo-1-propyl-dec-2-enyl)-carbamate
CAS NO:883559-62-4
Molecular Formula:
Molecular Weight: 461.642
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: tert-butyl (1R,2Z,6R,7R,9R)-(10-benzyloxy-6-hydroxy-7,9-dimethyl-8-oxo-1-propyl-dec-2-enyl)-carbamate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl (1R,2Z,6R,7R,9R)-(10-benzyloxy-6-hydroxy-7,9-dimethyl-8-oxo-1-propyl-dec-2-enyl)-carbamate(883559-62-4)
EPA Substance Registry System: tert-butyl (1R,2Z,6R,7R,9R)-(10-benzyloxy-6-hydroxy-7,9-dimethyl-8-oxo-1-propyl-dec-2-enyl)-carbamate(883559-62-4)

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: 883559-62-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 883559-62-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,3,5,5 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 883559-62:
(8*8)+(7*8)+(6*3)+(5*5)+(4*5)+(3*9)+(2*6)+(1*2)=224
224 % 10 = 4
So 883559-62-4 is a valid CAS Registry Number.

883559-62-4Upstream product

883559-62-4Downstream Products

883559-62-4Relevant academic research and scientific papers

The total synthesis of pamamycin-607. Part 2: Synthesis of the C6-C18 domain

Fraser, Benjamin H.,Mulder, Roger J.,Perlmutter, Patrick

, p. 2857 - 2867 (2007/10/03)

Synthesis of the C6-C18 domain of pamamycin-607 was achieved in ten steps and 7% overall yield from commercially available d-norvaline. The key asymmetric transformations included a Paterson anti aldol addition, an anti selective reduction of the resultan

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