Cas 98120-39-9,Benzoic acid (S)-2-bromo-1-((2S,3S,4S)-4-bromo-3-hydroxy-5-oxo-tetrahydro-furan-2-yl)-ethyl ester

98120-39-9

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Basic information

Product Name: Benzoic acid (S)-2-bromo-1-((2S,3S,4S)-4-bromo-3-hydroxy-5-oxo-tetrahydro-furan-2-yl)-ethyl ester
Synonyms: Benzoic acid (S)-2-bromo-1-((2S,3S,4S)-4-bromo-3-hydroxy-5-oxo-tetrahydro-furan-2-yl)-ethyl ester
CAS NO:98120-39-9
Molecular Formula:
Molecular Weight: 408.043
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: Benzoic acid (S)-2-bromo-1-((2S,3S,4S)-4-bromo-3-hydroxy-5-oxo-tetrahydro-furan-2-yl)-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid (S)-2-bromo-1-((2S,3S,4S)-4-bromo-3-hydroxy-5-oxo-tetrahydro-furan-2-yl)-ethyl ester(98120-39-9)
EPA Substance Registry System: Benzoic acid (S)-2-bromo-1-((2S,3S,4S)-4-bromo-3-hydroxy-5-oxo-tetrahydro-furan-2-yl)-ethyl ester(98120-39-9)

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: 98120-39-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 98120-39-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,1,2 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 98120-39:
(7*9)+(6*8)+(5*1)+(4*2)+(3*0)+(2*3)+(1*9)=139
139 % 10 = 9
So 98120-39-9 is a valid CAS Registry Number.

98120-39-9Upstream product

98120-39-9Downstream Products

98120-40-2 5-O-benzoyl-2,6-dibromo-2,6-dideoxy-3-O-methoxymethyl-D-mannono-1,4-lactone

98120-39-9Relevant academic research and scientific papers

SYNTHESIS AND PHOTOLYSIS OF SOME CARBOHYDRATE 1,6-DIENES

Ferrier, Robert J.,Tyler, Peter C.

, p. 249 - 258 (1985)

Several attempts to abbreviate our earlier syntheses of the prostaglandin intermediates 4 and 5 by photocyclisation of carbohydrate-based 1,6-dienes (15-18, 20, 22) did not yield the required bicycloheptane derivatives.Photolysis of 7-O-tert-butyld

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