Cas 1601389-76-7,(S)-4-(4-methoxyphenyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pentan-2-one

1601389-76-7

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Basic information

Product Name: (S)-4-(4-methoxyphenyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pentan-2-one
Synonyms: (S)-4-(4-methoxyphenyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pentan-2-one
CAS NO:1601389-76-7
Molecular Formula:
Molecular Weight: 318.221
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: (S)-4-(4-methoxyphenyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pentan-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-4-(4-methoxyphenyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pentan-2-one(1601389-76-7)
EPA Substance Registry System: (S)-4-(4-methoxyphenyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pentan-2-one(1601389-76-7)

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: 1601389-76-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1601389-76-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,1,3,8 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1601389-76:
(9*1)+(8*6)+(7*0)+(6*1)+(5*3)+(4*8)+(3*9)+(2*7)+(1*6)=157
157 % 10 = 7
So 1601389-76-7 is a valid CAS Registry Number.

1601389-76-7Upstream product

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1601389-76-7Relevant academic research and scientific papers

Enantioselective synthesis of boron-substituted quaternary carbon stereogenic centers through NHC-catalyzed conjugate additions of (pinacolato)boron units to enones

Radomkit, Suttipol,Hoveyda, Amir H.

supporting information, p. 3387 - 3391 (2014/04/03)

The first examples of Lewis base catalyzed enantioselective boryl conjugate additions (BCAs) that generate products containing boron-substituted quaternary carbon stereogenic centers are disclosed. Reactions are performed in the presence of 1.0-5.0 mol %

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