Cas 1040282-48-1,2-O-acetyl-3,4,6-tri-O-benzyl-1-O-(N-phenyltrifluoroacetimidoyl)-α-D-mannopyranoside

1040282-48-1

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Basic information

Product Name: 2-O-acetyl-3,4,6-tri-O-benzyl-1-O-(N-phenyltrifluoroacetimidoyl)-α-D-mannopyranoside
Synonyms: 2-O-acetyl-3,4,6-tri-O-benzyl-1-O-(N-phenyltrifluoroacetimidoyl)-α-D-mannopyranoside
CAS NO:1040282-48-1
Molecular Formula:
Molecular Weight: 663.691
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: 2-O-acetyl-3,4,6-tri-O-benzyl-1-O-(N-phenyltrifluoroacetimidoyl)-α-D-mannopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: 2-O-acetyl-3,4,6-tri-O-benzyl-1-O-(N-phenyltrifluoroacetimidoyl)-α-D-mannopyranoside(1040282-48-1)
EPA Substance Registry System: 2-O-acetyl-3,4,6-tri-O-benzyl-1-O-(N-phenyltrifluoroacetimidoyl)-α-D-mannopyranoside(1040282-48-1)

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: 1040282-48-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1040282-48-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,0,2,8 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1040282-48:
(9*1)+(8*0)+(7*4)+(6*0)+(5*2)+(4*8)+(3*2)+(2*4)+(1*8)=101
101 % 10 = 1
So 1040282-48-1 is a valid CAS Registry Number.

1040282-48-1Upstream product

1040282-48-1Downstream Products

1040282-25-4 C₈₆H₉₂O₁₆

1040282-48-1Relevant academic research and scientific papers

Targeted delivery of fluorescent high-mannose-type oligosaccharide cathepsin inhibitor conjugates

Wong, Chung S.,Hoogendoorn, Sascha,Van Der Marel, Gijs A.,Overkleeft, Herman S.,Codée, Jeroen D. C.

, p. 928 - 937 (2015)

Abstract Three fluorescent cathepsin inhibitor glycoconjugates have been designed, synthesized, and evaluated in terms of their cell internalization and cathepsin inhibitory properties. The conjugates are composed of a peptide epoxysuccinate, capable of c

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