Cas 1055324-11-2,4-[4-(benzyloxy)phenyl]-1-[(4R,6R)-2,2-dimethyl-4-tridecyl-1,3-dioxan-4-yl]-3-butyn-2-ol

1055324-11-2

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Basic information

Product Name: 4-[4-(benzyloxy)phenyl]-1-[(4R,6R)-2,2-dimethyl-4-tridecyl-1,3-dioxan-4-yl]-3-butyn-2-ol
Synonyms: 4-[4-(benzyloxy)phenyl]-1-[(4R,6R)-2,2-dimethyl-4-tridecyl-1,3-dioxan-4-yl]-3-butyn-2-ol
CAS NO:1055324-11-2
Molecular Formula:
Molecular Weight: 548.806
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: 4-[4-(benzyloxy)phenyl]-1-[(4R,6R)-2,2-dimethyl-4-tridecyl-1,3-dioxan-4-yl]-3-butyn-2-ol(CAS DataBase Reference)
NIST Chemistry Reference: 4-[4-(benzyloxy)phenyl]-1-[(4R,6R)-2,2-dimethyl-4-tridecyl-1,3-dioxan-4-yl]-3-butyn-2-ol(1055324-11-2)
EPA Substance Registry System: 4-[4-(benzyloxy)phenyl]-1-[(4R,6R)-2,2-dimethyl-4-tridecyl-1,3-dioxan-4-yl]-3-butyn-2-ol(1055324-11-2)

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: 1055324-11-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1055324-11-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,5,3,2 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1055324-11:
(9*1)+(8*0)+(7*5)+(6*5)+(5*3)+(4*2)+(3*4)+(2*1)+(1*1)=112
112 % 10 = 2
So 1055324-11-2 is a valid CAS Registry Number.

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1055324-11-2Relevant academic research and scientific papers

Total synthesis of aculeatins A and B from d-glucose

Suresh, Vangaru,Jon Paul Selvam, Jondoss,Rajesh, Karuturi,Venkateswarlu, Yenamandra

, p. 1508 - 1512 (2008)

A simple and highly efficient total synthesis of cytotoxic dioxa-dispiroketals aculeatins A and B is disclosed. The key steps include alkynylation of a chiral aldehyde and in situ deprotection, spirocyclization of a 3,5-acetonide protected ketone.

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