Cas 158774-76-6,methyl (E)-<6-2H>-2,3,4-tri-O-benzyl-6-deoxy-α-D-xylo-hex-5-enopyranoside

158774-76-6

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Basic information

Product Name: methyl (E)-<6-2H>-2,3,4-tri-O-benzyl-6-deoxy-α-D-xylo-hex-5-enopyranoside
Synonyms: methyl (E)-<6-2H>-2,3,4-tri-O-benzyl-6-deoxy-α-D-xylo-hex-5-enopyranoside
CAS NO:158774-76-6
Molecular Formula:
Molecular Weight: 447.535
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: methyl (E)-<6-2H>-2,3,4-tri-O-benzyl-6-deoxy-α-D-xylo-hex-5-enopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: methyl (E)-<6-2H>-2,3,4-tri-O-benzyl-6-deoxy-α-D-xylo-hex-5-enopyranoside(158774-76-6)
EPA Substance Registry System: methyl (E)-<6-2H>-2,3,4-tri-O-benzyl-6-deoxy-α-D-xylo-hex-5-enopyranoside(158774-76-6)

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: 158774-76-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 158774-76-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,7,7 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 158774-76:
(8*1)+(7*5)+(6*8)+(5*7)+(4*7)+(3*4)+(2*7)+(1*6)=186
186 % 10 = 6
So 158774-76-6 is a valid CAS Registry Number.

158774-76-6Upstream product

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158774-76-6Relevant academic research and scientific papers

Mechanistic and stereochemical studies on Ferrier reaction by means of chirally deuterated glucose

Yamauchi, Noriaki,Terachi, Takumi,Eguchi, Tadashi,Kakinuma, Katsumi

, p. 4125 - 4136 (2007/10/02)

The mechanism of Ferrier reaction, cyclitol formation from 5-enopyranosides, was investigated by using (E)-selectively deuterated methyl [6-2H]-2,3,4-tri-O-benzyl-α-D-xylo-hex-5-enopyranoside. The overall reaction was non-stereoselective with r

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