Cas 129885-85-4,(1R,2S,6S,7R,8R)-7-((2R,4R,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-4,4-dimethyl-3,5,9,11-tetraoxa-tricyclo[6.2.1.0<sup>2,6</sup>]undecane

129885-85-4

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Basic information

Product Name: (1R,2S,6S,7R,8R)-7-((2R,4R,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-4,4-dimethyl-3,5,9,11-tetraoxa-tricyclo[6.2.1.0^2,6]undecane
Synonyms:
CAS NO:129885-85-4
Molecular Formula:
Molecular Weight: 618.724
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: (1R,2S,6S,7R,8R)-7-((2R,4R,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-4,4-dimethyl-3,5,9,11-tetraoxa-tricyclo[6.2.1.0^2,6]undecane(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2S,6S,7R,8R)-7-((2R,4R,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-4,4-dimethyl-3,5,9,11-tetraoxa-tricyclo[6.2.1.0^2,6]undecane(129885-85-4)
EPA Substance Registry System: (1R,2S,6S,7R,8R)-7-((2R,4R,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-4,4-dimethyl-3,5,9,11-tetraoxa-tricyclo[6.2.1.0^2,6]undecane(129885-85-4)

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: 129885-85-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 129885-85-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,8,8 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 129885-85:
(8*1)+(7*2)+(6*9)+(5*8)+(4*8)+(3*5)+(2*8)+(1*5)=184
184 % 10 = 4
So 129885-85-4 is a valid CAS Registry Number.

129885-85-4Upstream product

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129885-85-4Relevant academic research and scientific papers

A Convenient 2-Deoxy-α-D-glucopyranosylation Reaction Using Dimethylphosphinothioate Method

Yamanoi, Takashi,Inazu, Toshiyuki

, p. 849 - 852 (1990)

Several 2-deoxy-α-glucosides were obtained in good yields with high stereoselectivity by glycosylation reaction of the corresponding alcohols with 3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranosyl dimethylphosphinothioate in the presence of a catalytic amount of triphenylmethylium perchlorate or an equivalent amount of silver perchlorate.

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