Cas 1300698-99-0,(5R,6S)-5-bromo-6-(4-chlorophenyl)tetrahydro-2H-pyran-2-one

1300698-99-0

Post Buying Request

Basic information

Product Name: (5R,6S)-5-bromo-6-(4-chlorophenyl)tetrahydro-2H-pyran-2-one
Synonyms: (5R,6S)-5-bromo-6-(4-chlorophenyl)tetrahydro-2H-pyran-2-one
CAS NO:1300698-99-0
Molecular Formula:
Molecular Weight: 289.556
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: (5R,6S)-5-bromo-6-(4-chlorophenyl)tetrahydro-2H-pyran-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (5R,6S)-5-bromo-6-(4-chlorophenyl)tetrahydro-2H-pyran-2-one(1300698-99-0)
EPA Substance Registry System: (5R,6S)-5-bromo-6-(4-chlorophenyl)tetrahydro-2H-pyran-2-one(1300698-99-0)

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: 1300698-99-0(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

1300698-99-0 Suppliers

Recommended suppliers

1300698-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1300698-99-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,0,6,9 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1300698-99:
(9*1)+(8*3)+(7*0)+(6*0)+(5*6)+(4*9)+(3*8)+(2*9)+(1*9)=150
150 % 10 = 0
So 1300698-99-0 is a valid CAS Registry Number.

1300698-99-0Upstream product

5724-02-7 trans-5-(p-chloro-phenyl)-pent-4-enoic acid

1300698-99-0Downstream Products

1300698-99-0Relevant academic research and scientific papers

Aminothiocarbamate-catalyzed asymmetric bromolactonization of 1,2-disubstituted olefinic acids

Tan, Chong Kiat,Zhou, Ling,Yeung, Ying-Yeung

, p. 2738 - 2741 (2011)

An efficient and enantioselective bromolactonization of 1,2-disubstituted olefinic acids using an amino-thiocarbamate catalyst has been developed, resulting in the formation of δ-lactones containing two chiral centers with up to 99% yield, 95% ee.

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 1300698-99-0