Cas 135388-52-2,3-(4-Chloro-phenyl)-N-methoxy-N-methyl-3-trimethylsilanyloxy-propionamide

135388-52-2

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Basic information

Product Name: 3-(4-Chloro-phenyl)-N-methoxy-N-methyl-3-trimethylsilanyloxy-propionamide
Synonyms: 3-(4-Chloro-phenyl)-N-methoxy-N-methyl-3-trimethylsilanyloxy-propionamide
CAS NO:135388-52-2
Molecular Formula:
Molecular Weight: 315.872
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: 3-(4-Chloro-phenyl)-N-methoxy-N-methyl-3-trimethylsilanyloxy-propionamide(CAS DataBase Reference)
NIST Chemistry Reference: 3-(4-Chloro-phenyl)-N-methoxy-N-methyl-3-trimethylsilanyloxy-propionamide(135388-52-2)
EPA Substance Registry System: 3-(4-Chloro-phenyl)-N-methoxy-N-methyl-3-trimethylsilanyloxy-propionamide(135388-52-2)

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: 135388-52-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 135388-52-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,3,8 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 135388-52:
(8*1)+(7*3)+(6*5)+(5*3)+(4*8)+(3*8)+(2*5)+(1*2)=142
142 % 10 = 2
So 135388-52-2 is a valid CAS Registry Number.

135388-52-2Upstream product

135388-52-2Downstream Products

135388-57-7 1-(4-Chloro-phenyl)-1-trimethylsilanyloxy-pentan-3-one

135388-52-2Relevant academic research and scientific papers

Regiocontrol synthesis of β-trimetylsilyloxy carbonyl compounds through an aldolgrignard elaboration sequence

Palomo, Caludio,Aizpurua, Jesus M.,Aurrejoetxea, Natalia,Lopez, M. Conception

, p. 2525 - 2528 (2007/10/02)

Reaction of carbonyl compounds with α-lithio- or α-halozinc N-methoxy-N-methylamides, followed by silylation and Grignard addition resulted in a regiocontrolled synthesis of β-trimethylsilyloxy carbonyl compounds.

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