Cas 135253-85-9,Acetic acid (2R,3S,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-(4-acryloylamino-phenoxy)-tetrahydro-pyran-4-yl ester

135253-85-9

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Basic information

Product Name: Acetic acid (2R,3S,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-(4-acryloylamino-phenoxy)-tetrahydro-pyran-4-yl ester
Synonyms: Acetic acid (2R,3S,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-(4-acryloylamino-phenoxy)-tetrahydro-pyran-4-yl ester
CAS NO:135253-85-9
Molecular Formula:
Molecular Weight: 492.483
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: Acetic acid (2R,3S,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-(4-acryloylamino-phenoxy)-tetrahydro-pyran-4-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (2R,3S,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-(4-acryloylamino-phenoxy)-tetrahydro-pyran-4-yl ester(135253-85-9)
EPA Substance Registry System: Acetic acid (2R,3S,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-(4-acryloylamino-phenoxy)-tetrahydro-pyran-4-yl ester(135253-85-9)

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: 135253-85-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 135253-85-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,2,5 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 135253-85:
(8*1)+(7*3)+(6*5)+(5*2)+(4*5)+(3*3)+(2*8)+(1*5)=119
119 % 10 = 9
So 135253-85-9 is a valid CAS Registry Number.

135253-85-9Upstream product

135253-85-9Downstream Products

135253-87-1 p-Acryloylaminophenyl 2-acetamido-2-deoxy-β-D-glucopyranoside

135253-85-9Relevant academic research and scientific papers

Syntheses and Transformations of Glycohydrolase Substrates into Protein Conjugates Based on Michael Additions

Roy, Rene,Tropper, Francois D.,Morrison, Tara,Boratynski, Janusz

, p. 536 - 538 (2007/10/02)

The glycosyl chloride 1 and bromides 2 and 3 were stereospecifically transformed into p-nitrophenyl glycosides by phase transfer catalysis; these glycohydrolase substrates were reduced and N-acryloylated to afford Michael acceptors which reacted with amine functions of proteins.

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