Cas 1332305-22-2,methyl N-(9-fluorenylmethoxycarbonyl)-O-[2,3,6-tri-O-benzoyl-4-O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-β-D-glucopyranosyl]-L-threoninate

1332305-22-2

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Basic information

Product Name: methyl N-(9-fluorenylmethoxycarbonyl)-O-[2,3,6-tri-O-benzoyl-4-O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-β-D-glucopyranosyl]-L-threoninate
Synonyms: methyl N-(9-fluorenylmethoxycarbonyl)-O-[2,3,6-tri-O-benzoyl-4-O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-β-D-glucopyranosyl]-L-threoninate
CAS NO:1332305-22-2
Molecular Formula:
Molecular Weight: 1408.43
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 N-(9-fluorenylmethoxycarbonyl)-O-[2,3,6-tri-O-benzoyl-4-O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-β-D-glucopyranosyl]-L-threoninate(CAS DataBase Reference)
NIST Chemistry Reference: methyl N-(9-fluorenylmethoxycarbonyl)-O-[2,3,6-tri-O-benzoyl-4-O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-β-D-glucopyranosyl]-L-threoninate(1332305-22-2)
EPA Substance Registry System: methyl N-(9-fluorenylmethoxycarbonyl)-O-[2,3,6-tri-O-benzoyl-4-O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-β-D-glucopyranosyl]-L-threoninate(1332305-22-2)

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: 1332305-22-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1332305-22-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,2,3,0 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1332305-22:
(9*1)+(8*3)+(7*3)+(6*2)+(5*3)+(4*0)+(3*5)+(2*2)+(1*2)=102
102 % 10 = 2
So 1332305-22-2 is a valid CAS Registry Number.

1332305-22-2Upstream product

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1332305-22-2Relevant academic research and scientific papers

Facile synthesis of unusual glycosyl carbamates and amino acid glycosides from propargyl 1,2-orthoesters as glycosyl donors

Shaikh, Ashif Y.,Sureshkumar, Gopalsamy,Pati, Debasish,Gupta, Sayam Sen,Hotha, Srinivas

supporting information; experimental part, p. 5951 - 5959 (2011/10/09)

Propargyl 1,2-O-orthoesters are exploited for the synthesis of 1,2-trans O-glycosides of protected amino acids. N-Fmoc- and N-Cbz protected serine/threonine - benzyl/methyl esters reacted well with glucosyl-, galactosyl-, mannosyl- and lactosyl- derived propargyl 1,2-orthoesters affording respective 1,2-trans glycosides in good yields under AuBr3/4 A MS Powder/CH2Cl2/rt. t-Boc serine derivative gave serine 1,2-orthoester and glycosyl carbamate. Optimized conditions enabled preparation of new glycosyl carbamates from N-Boc protected amines in a single step using gold catalysts and propargyl 1,2-orthoesters in excellent yields.

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