Cas 138560-31-3,(-)-(3aα,4α,5β,6α,7β)-3,3a,4,5,6,7-hexahydro-7-<(4-methoxyphenyl)methoxy>-4,5,6-tris(phenylmethoxy)-2,1-benzisoxazole

138560-31-3

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Basic information

Product Name: (-)-(3aα,4α,5β,6α,7β)-3,3a,4,5,6,7-hexahydro-7-<(4-methoxyphenyl)methoxy>-4,5,6-tris(phenylmethoxy)-2,1-benzisoxazole
Synonyms:
CAS NO:138560-31-3
Molecular Formula:
Molecular Weight: 579.693
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: (-)-(3aα,4α,5β,6α,7β)-3,3a,4,5,6,7-hexahydro-7-<(4-methoxyphenyl)methoxy>-4,5,6-tris(phenylmethoxy)-2,1-benzisoxazole(CAS DataBase Reference)
NIST Chemistry Reference: (-)-(3aα,4α,5β,6α,7β)-3,3a,4,5,6,7-hexahydro-7-<(4-methoxyphenyl)methoxy>-4,5,6-tris(phenylmethoxy)-2,1-benzisoxazole(138560-31-3)
EPA Substance Registry System: (-)-(3aα,4α,5β,6α,7β)-3,3a,4,5,6,7-hexahydro-7-<(4-methoxyphenyl)methoxy>-4,5,6-tris(phenylmethoxy)-2,1-benzisoxazole(138560-31-3)

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: 138560-31-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 138560-31-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,5,6 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 138560-31:
(8*1)+(7*3)+(6*8)+(5*5)+(4*6)+(3*0)+(2*3)+(1*1)=133
133 % 10 = 3
So 138560-31-3 is a valid CAS Registry Number.

138560-31-3Upstream product

138560-26-6 6,7-dideoxy-2-<(4-methoxyphenyl)methoxy>-3,4,5-tris-O-(phenylmethyl)-D-gulo/ido-hept-6-enose, cyclic 1,3-propanediyl mercaptals

138560-31-3Downstream Products

138560-31-3Relevant academic research and scientific papers

Diastereoselectivity in the intramolecular nitrone, oxime, and nitrile oxide cycloaddition reactions. Synthesis of amino inositol derivatives as α-glucosidase inhibitors

Peet, Norton P.,Huber, Edward W.,Farr, Robert A.

, p. 7537 - 7550 (1991)

The diastereoselectivity in the intramolecular 1,3-dipolar cycloaddition reactions of 4 and 5 (R=Bn, 4-MeOBn) was examined.

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