Cas 1384251-53-9,(trifluoromethyl)(2-nitro-5-chlorophenyl)methyl 4,6-di-O-acetyl-2,3-dideoxy-α-D-erythrohex-2-enopyranoside

1384251-53-9

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Basic information

Product Name: (trifluoromethyl)(2-nitro-5-chlorophenyl)methyl 4,6-di-O-acetyl-2,3-dideoxy-α-D-erythrohex-2-enopyranoside
Synonyms: (trifluoromethyl)(2-nitro-5-chlorophenyl)methyl 4,6-di-O-acetyl-2,3-dideoxy-α-D-erythrohex-2-enopyranoside
CAS NO:1384251-53-9
Molecular Formula:
Molecular Weight: 467.783
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: (trifluoromethyl)(2-nitro-5-chlorophenyl)methyl 4,6-di-O-acetyl-2,3-dideoxy-α-D-erythrohex-2-enopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: (trifluoromethyl)(2-nitro-5-chlorophenyl)methyl 4,6-di-O-acetyl-2,3-dideoxy-α-D-erythrohex-2-enopyranoside(1384251-53-9)
EPA Substance Registry System: (trifluoromethyl)(2-nitro-5-chlorophenyl)methyl 4,6-di-O-acetyl-2,3-dideoxy-α-D-erythrohex-2-enopyranoside(1384251-53-9)

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: 1384251-53-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1384251-53-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,4,2,5 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1384251-53:
(9*1)+(8*3)+(7*8)+(6*4)+(5*2)+(4*5)+(3*1)+(2*5)+(1*3)=159
159 % 10 = 9
So 1384251-53-9 is a valid CAS Registry Number.

1384251-53-9Upstream product

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1384251-53-9Relevant academic research and scientific papers

Iron(III) triflate, a new efficient catalyst for Type i Ferrier Rearrangement

Chen, Peiran,Wang, Shaoshan

, p. 5356 - 5362 (2012)

By using iron(III) triflate as catalyst, an improved method for the synthesis of 2,3-unsaturated-O-glycosides has been established. A series of 2,3-unsaturated-O-glucosides were obtained from 2,4,6-tri-O-acetyl-d-glucal in good yield and high anomeric selectivity.

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