Cas 165805-40-3,2-Azidomethyl-benzoic acid (2S,3S,4R,5R,6S)-4-acetoxy-5-acetylamino-2-acetylsulfanylmethyl-6-allyloxy-tetrahydro-pyran-3-yl ester

165805-40-3

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Basic information

Product Name: 2-Azidomethyl-benzoic acid (2S,3S,4R,5R,6S)-4-acetoxy-5-acetylamino-2-acetylsulfanylmethyl-6-allyloxy-tetrahydro-pyran-3-yl ester
Synonyms: 2-Azidomethyl-benzoic acid (2S,3S,4R,5R,6S)-4-acetoxy-5-acetylamino-2-acetylsulfanylmethyl-6-allyloxy-tetrahydro-pyran-3-yl ester
CAS NO:165805-40-3
Molecular Formula:
Molecular Weight: 520.563
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-Azidomethyl-benzoic acid (2S,3S,4R,5R,6S)-4-acetoxy-5-acetylamino-2-acetylsulfanylmethyl-6-allyloxy-tetrahydro-pyran-3-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-Azidomethyl-benzoic acid (2S,3S,4R,5R,6S)-4-acetoxy-5-acetylamino-2-acetylsulfanylmethyl-6-allyloxy-tetrahydro-pyran-3-yl ester(165805-40-3)
EPA Substance Registry System: 2-Azidomethyl-benzoic acid (2S,3S,4R,5R,6S)-4-acetoxy-5-acetylamino-2-acetylsulfanylmethyl-6-allyloxy-tetrahydro-pyran-3-yl ester(165805-40-3)

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: 165805-40-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 165805-40-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,5,8,0 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 165805-40:
(8*1)+(7*6)+(6*5)+(5*8)+(4*0)+(3*5)+(2*4)+(1*0)=143
143 % 10 = 3
So 165805-40-3 is a valid CAS Registry Number.

165805-40-3Upstream product

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165805-40-3Relevant academic research and scientific papers

Regiospecific 4,6-functionalization of pyranosides via dimethylboron bromide-mediated cleavage of phthalide orthoesters

Arasappan, Ashok,Fuchs

, p. 177 - 183 (2007/10/02)

An efficient strategy for regiocontrolled differentiation of the 4,6-positions of pyranosides has been developed using dimethylboron bromide-mediated cleavage of phthalide orthoesters. The reaction proceeds under mild conditions, is tolerant of additional

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