Cas 1401695-38-2,phenyl 2-azido-2-deoxy-4-O-p-methoxybenzyl-1-thio-3-O-triisopropylsilyl-β-D-glucopyranose

1401695-38-2

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Basic information

Product Name: phenyl 2-azido-2-deoxy-4-O-p-methoxybenzyl-1-thio-3-O-triisopropylsilyl-β-D-glucopyranose
Synonyms: phenyl 2-azido-2-deoxy-4-O-p-methoxybenzyl-1-thio-3-O-triisopropylsilyl-β-D-glucopyranose
CAS NO:1401695-38-2
Molecular Formula:
Molecular Weight: 573.829
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: phenyl 2-azido-2-deoxy-4-O-p-methoxybenzyl-1-thio-3-O-triisopropylsilyl-β-D-glucopyranose(CAS DataBase Reference)
NIST Chemistry Reference: phenyl 2-azido-2-deoxy-4-O-p-methoxybenzyl-1-thio-3-O-triisopropylsilyl-β-D-glucopyranose(1401695-38-2)
EPA Substance Registry System: phenyl 2-azido-2-deoxy-4-O-p-methoxybenzyl-1-thio-3-O-triisopropylsilyl-β-D-glucopyranose(1401695-38-2)

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: 1401695-38-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1401695-38-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,1,6,9 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1401695-38:
(9*1)+(8*4)+(7*0)+(6*1)+(5*6)+(4*9)+(3*5)+(2*3)+(1*8)=142
142 % 10 = 2
So 1401695-38-2 is a valid CAS Registry Number.

1401695-38-2Upstream product

80522-42-5 triisopropylsilyl trifluoromethanesulfonate

1401695-38-2Downstream Products

1401695-38-2Relevant academic research and scientific papers

Synthesis of a benzomacrolactone-based somatostatin mimetic

Zhou, Jian,Matos, Marie-Christine,Murphy, Paul V.

, p. 5716 - 5719 (2011/12/05)

The benzomacrolactone is a framework found in numerous natural products. The synthesis of an orthogonally functionalized benzomacrolactone from d-glucosamine and a salicylic acid derivative is described. This macrolactone was used for the synthesis of a somatostatin mimetic that has submicromolar affinity for the human somatostatin receptor 4 (hSSTR4).

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