Cas 669081-24-7,Acetamide, N-[(1S)-1-(3,4-dimethoxyphenyl)-3-butenyl]-2,2,2-trifluoro-N-[(4S)-2-oxo -4-(phenylmethyl)-3-oxazolidinyl]-

669081-24-7

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Basic information

Product Name: Acetamide, N-[(1S)-1-(3,4-dimethoxyphenyl)-3-butenyl]-2,2,2-trifluoro-N-[(4S)-2-oxo -4-(phenylmethyl)-3-oxazolidinyl]-
Synonyms:
CAS NO:669081-24-7
Molecular Formula: C24H25F3N2O5
Molecular Weight: 478.468
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: Acetamide, N-[(1S)-1-(3,4-dimethoxyphenyl)-3-butenyl]-2,2,2-trifluoro-N-[(4S)-2-oxo -4-(phenylmethyl)-3-oxazolidinyl]-(CAS DataBase Reference)
NIST Chemistry Reference: Acetamide, N-[(1S)-1-(3,4-dimethoxyphenyl)-3-butenyl]-2,2,2-trifluoro-N-[(4S)-2-oxo -4-(phenylmethyl)-3-oxazolidinyl]-(669081-24-7)
EPA Substance Registry System: Acetamide, N-[(1S)-1-(3,4-dimethoxyphenyl)-3-butenyl]-2,2,2-trifluoro-N-[(4S)-2-oxo -4-(phenylmethyl)-3-oxazolidinyl]-(669081-24-7)

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: 669081-24-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 669081-24-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,9,0,8 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 669081-24:
(8*6)+(7*6)+(6*9)+(5*0)+(4*8)+(3*1)+(2*2)+(1*4)=187
187 % 10 = 7
So 669081-24-7 is a valid CAS Registry Number.

669081-24-7Upstream product

669081-24-7Downstream Products

669081-24-7Relevant academic research and scientific papers

Trifluoroacetyl-Activated Nitrogen-Nitrogen Bond Cleavage of Hydrazines by Samarium(II) Iodide

Ding, Hui,Friestad, Gregory K.

, p. 637 - 640 (2004)

(Matrix presented) Trifluoroacetyl derivatives of hydrazines undergo clean and efficient reductive cleavage of the N-N bond with Sml2 in the presence of MeOH. After N-trifluoroacetylation, acyl-, aryl-, and alkyl-substituted hydrazines are redu

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