Cas 1601389-62-1,(S)-3-(naphthalen-2-yl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohexan-1-one

1601389-62-1

Post Buying Request

Basic information

Product Name: (S)-3-(naphthalen-2-yl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohexan-1-one
Synonyms: (S)-3-(naphthalen-2-yl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohexan-1-one
CAS NO:1601389-62-1
Molecular Formula:
Molecular Weight: 350.266
EINECS: N/A
Product Categories: N/A
Mol File: 1601389-62-1.mol
Article Data: 1

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)-3-(naphthalen-2-yl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohexan-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-3-(naphthalen-2-yl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohexan-1-one(1601389-62-1)
EPA Substance Registry System: (S)-3-(naphthalen-2-yl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohexan-1-one(1601389-62-1)

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: 1601389-62-1(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

1601389-62-1 Suppliers

Recommended suppliersmore

1601389-62-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1601389-62-1 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, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1601389-62:
(9*1)+(8*6)+(7*0)+(6*1)+(5*3)+(4*8)+(3*9)+(2*6)+(1*2)=151
151 % 10 = 1
So 1601389-62-1 is a valid CAS Registry Number.

1601389-62-1Upstream product

1601389-62-1Downstream Products

1601389-62-1Relevant articles and documents

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 %

Post a RFQ

Cas No.:

Product Name:

Quantity:

Email:

Company name:

Valid Period:

Detailed Requirements:

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

What can I do for you?
Get Best Price

Get Best Price for 1601389-62-1