Cas 124738-89-2,(5R)-1,2-O-isopropylidene-3-O-methyl-5-(2-hydroxy-5-tert-butylphenyl)-α-D-xylofuranose

124738-89-2

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Basic information

Product Name: (5R)-1,2-O-isopropylidene-3-O-methyl-5-(2-hydroxy-5-tert-butylphenyl)-α-D-xylofuranose
Synonyms:
CAS NO:124738-89-2
Molecular Formula:
Molecular Weight: 352.428
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: (5R)-1,2-O-isopropylidene-3-O-methyl-5-(2-hydroxy-5-tert-butylphenyl)-α-D-xylofuranose(CAS DataBase Reference)
NIST Chemistry Reference: (5R)-1,2-O-isopropylidene-3-O-methyl-5-(2-hydroxy-5-tert-butylphenyl)-α-D-xylofuranose(124738-89-2)
EPA Substance Registry System: (5R)-1,2-O-isopropylidene-3-O-methyl-5-(2-hydroxy-5-tert-butylphenyl)-α-D-xylofuranose(124738-89-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
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Hazardous Substances Data: 124738-89-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 124738-89-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,7,3 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 124738-89:
(8*1)+(7*2)+(6*4)+(5*7)+(4*3)+(3*8)+(2*8)+(1*9)=142
142 % 10 = 2
So 124738-89-2 is a valid CAS Registry Number.

124738-89-2Upstream product

124738-89-2Downstream Products

124738-89-2Relevant academic research and scientific papers

STEREOSELECTIVE ARYLATIONS USING METAL PHENOLATES. COMPLEMENTARY SYNTHESIS OF 5-C-ARYLXYLOFURANOSE DERIVATIVES OF EITHER L-IDO OR D-GLUCO CONFIGURATION

Cornia, Mara,Casiraghi, Giovanni

, p. 2869 - 2874 (2007/10/02)

The arylation of 3-O-methyl-1,2-O-isopropylidene-α-D-xylo-pentodialdofuranose (2) at the aldehyde centre by means of bromomagnesium or triisopropoxytitanium salts of phenols 1 provides a simple access to 5-C arylxylofuranoses 3 and 4 of either L-ido or D-

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