Cas 1423809-90-8,(4R)-4-benzyl-3-(4,4,4-trifluoro-3-(nitromethyl)butanoyl)oxazolidin-2-one

1423809-90-8

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Basic information

Product Name: (4R)-4-benzyl-3-(4,4,4-trifluoro-3-(nitromethyl)butanoyl)oxazolidin-2-one
Synonyms: (4R)-4-benzyl-3-(4,4,4-trifluoro-3-(nitromethyl)butanoyl)oxazolidin-2-one
CAS NO:1423809-90-8
Molecular Formula:
Molecular Weight: 360.29
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: (4R)-4-benzyl-3-(4,4,4-trifluoro-3-(nitromethyl)butanoyl)oxazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (4R)-4-benzyl-3-(4,4,4-trifluoro-3-(nitromethyl)butanoyl)oxazolidin-2-one(1423809-90-8)
EPA Substance Registry System: (4R)-4-benzyl-3-(4,4,4-trifluoro-3-(nitromethyl)butanoyl)oxazolidin-2-one(1423809-90-8)

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: 1423809-90-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1423809-90-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,3,8,0 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1423809-90:
(9*1)+(8*4)+(7*2)+(6*3)+(5*8)+(4*0)+(3*9)+(2*9)+(1*0)=158
158 % 10 = 8
So 1423809-90-8 is a valid CAS Registry Number.

1423809-90-8Upstream product

75-52-5 nitromethane

1423809-90-8Downstream Products

1423809-90-8Relevant academic research and scientific papers

Enantioselective organocatalytic michael addition of nitroalkanes and other nucleophiles to β-trifluoromethylated acrylamides

Wen, Lele,Yin, Liang,Shen, Qilong,Lu, Long

, p. 502 - 506 (2013)

An organocatalytic asymmetric Michael addition of nitroalkanes to trifluoromethylated acrylamides in good yields and with good to excellent diastereoselectivities and excellent enantioselectivities is described. The Michael adducts could be readily transf

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