Cas 234754-52-0,(3R,4aR,8R,8aR)-3-(5-Bromo-furan-2-yl)-8-isopropyl-5-methyl-3,4,4a,7,8,8a-hexahydro-isochromen-1-one

234754-52-0

Post Buying Request

Basic information

Product Name: (3R,4aR,8R,8aR)-3-(5-Bromo-furan-2-yl)-8-isopropyl-5-methyl-3,4,4a,7,8,8a-hexahydro-isochromen-1-one
Synonyms: (3R,4aR,8R,8aR)-3-(5-Bromo-furan-2-yl)-8-isopropyl-5-methyl-3,4,4a,7,8,8a-hexahydro-isochromen-1-one
CAS NO:234754-52-0
Molecular Formula:
Molecular Weight: 353.256
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: (3R,4aR,8R,8aR)-3-(5-Bromo-furan-2-yl)-8-isopropyl-5-methyl-3,4,4a,7,8,8a-hexahydro-isochromen-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (3R,4aR,8R,8aR)-3-(5-Bromo-furan-2-yl)-8-isopropyl-5-methyl-3,4,4a,7,8,8a-hexahydro-isochromen-1-one(234754-52-0)
EPA Substance Registry System: (3R,4aR,8R,8aR)-3-(5-Bromo-furan-2-yl)-8-isopropyl-5-methyl-3,4,4a,7,8,8a-hexahydro-isochromen-1-one(234754-52-0)

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: 234754-52-0(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

234754-52-0 Suppliers

Recommended suppliers

234754-52-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 234754-52-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,4,7,5 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 234754-52:
(8*2)+(7*3)+(6*4)+(5*7)+(4*5)+(3*4)+(2*5)+(1*2)=140
140 % 10 = 0
So 234754-52-0 is a valid CAS Registry Number.

234754-52-0Upstream product

234754-52-0Downstream Products

234754-52-0Relevant academic research and scientific papers

The total synthesis of eleutherobin

Chen, Xiao-Tao,Bhattacharya, Samit K.,Zhou, Bishan,Gutteridge, Clare E.,Pettus, Thomas R. R.,Danishefsky, Samuel J.

, p. 6563 - 6579 (2007/10/03)

The total synthesis of the title compound (1), starting with (R)-( - )-α-phellandrene (6), has been accomplished. The synthesis rigorously proves the relative stereochemical relationship of the diterpenoid and carbohydrate domains of eleutherobin. Key reactions included a Nozaki - Kishi ring closure to produce a furanophane (see 37 → 38), a pyranose to furanose transposition (see 50 → 47), and a novel oxycarbaglycosidation (cf. 58 → 87) for joining the two domains.

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 234754-52-0