Cas 1333121-74-6,methyl 6-[5a-carba-α-D-xylo-hex-5(5a)-enopyranosylamino]-6-deoxy-α-D-glucopyranoside

1333121-74-6

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Basic information

Product Name: methyl 6-[5a-carba-α-D-xylo-hex-5(5a)-enopyranosylamino]-6-deoxy-α-D-glucopyranoside
Synonyms: methyl 6-[5a-carba-α-D-xylo-hex-5(5a)-enopyranosylamino]-6-deoxy-α-D-glucopyranoside
CAS NO:1333121-74-6
Molecular Formula:
Molecular Weight: 351.354
EINECS: N/A
Product Categories: N/A
Mol File: 1333121-74-6.mol
Article Data: 1

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 6-[5a-carba-α-D-xylo-hex-5(5a)-enopyranosylamino]-6-deoxy-α-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: methyl 6-[5a-carba-α-D-xylo-hex-5(5a)-enopyranosylamino]-6-deoxy-α-D-glucopyranoside(1333121-74-6)
EPA Substance Registry System: methyl 6-[5a-carba-α-D-xylo-hex-5(5a)-enopyranosylamino]-6-deoxy-α-D-glucopyranoside(1333121-74-6)

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: 1333121-74-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1333121-74-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,3,1,2 and 1 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1333121-74:
(9*1)+(8*3)+(7*3)+(6*3)+(5*1)+(4*2)+(3*1)+(2*7)+(1*4)=106
106 % 10 = 6
So 1333121-74-6 is a valid CAS Registry Number.

1333121-74-6Upstream product

1332641-39-0 C₆₃H₆₇NO₉

1333121-74-6Downstream Products

1333121-74-6Relevant articles and documents

Synthesis and α-Glucosidase II inhibitory activity of valienamine pseudodisaccharides relevant to N-glycan biosynthesis

Cumpstey, Ian,Ramstadius, Clinton,Eszter Borbas,Alonzi, Dominic S.,Butters, Terry D.

supporting information; experimental part, p. 5219 - 5223 (2011/10/09)

Valienol-derived allylic C-1 bromides have been used as carbaglycosyl donors for α-xylo configured valienamine pseudodisaccharide synthesis. We synthesised valienamine analogues of the Glc(α1→3)Glc and Glc(α1→3)Man disaccharides representing the linkages

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