Cas 505030-55-7,(Z)-2-(2-Hydroxymethyl-piperidin-1-ylmethyl)-3-phenyl-acrylic acid methyl ester

505030-55-7

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Basic information

Product Name: (Z)-2-(2-Hydroxymethyl-piperidin-1-ylmethyl)-3-phenyl-acrylic acid methyl ester
Synonyms: (Z)-2-(2-Hydroxymethyl-piperidin-1-ylmethyl)-3-phenyl-acrylic acid methyl ester
CAS NO:505030-55-7
Molecular Formula:
Molecular Weight: 289.375
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: (Z)-2-(2-Hydroxymethyl-piperidin-1-ylmethyl)-3-phenyl-acrylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-2-(2-Hydroxymethyl-piperidin-1-ylmethyl)-3-phenyl-acrylic acid methyl ester(505030-55-7)
EPA Substance Registry System: (Z)-2-(2-Hydroxymethyl-piperidin-1-ylmethyl)-3-phenyl-acrylic acid methyl ester(505030-55-7)

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: 505030-55-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 505030-55-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,5,0,3 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 505030-55:
(8*5)+(7*0)+(6*5)+(5*0)+(4*3)+(3*0)+(2*5)+(1*5)=97
97 % 10 = 7
So 505030-55-7 is a valid CAS Registry Number.

505030-55-7Upstream product

505030-55-7Downstream Products

308358-15-8 (Z)-2-(2-Hydroxymethyl-piperidin-1-ylmethyl)-3-phenyl-acrylic acid

505030-55-7Relevant academic research and scientific papers

Synthesis of 1,4-oxazepin-7-ones using baylis-hillman products as key intermediates

Nilov, Dmitry,Raecker, Reinhard,Reiser, Oliver

, p. 2232 - 2242 (2002)

Baylis-Hilman adducts derived from aromatic aldehydes and methyl acrylate can be readily converted to 1,4-oxazepin-7-ones substituted in 2-, 3-, or 4-position by condensation with amino alcohols.

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