Cas 1026988-66-8,trans-N,N'-[2-(4'-fluoro-2'-methoxyphenyl)-cyclopent-3-enyl]-di-tert-butylhydrazine dicarboxylate

1026988-66-8

Post Buying Request

Basic information

Product Name: trans-N,N'-[2-(4'-fluoro-2'-methoxyphenyl)-cyclopent-3-enyl]-di-tert-butylhydrazine dicarboxylate
Synonyms: trans-N,N'-[2-(4'-fluoro-2'-methoxyphenyl)-cyclopent-3-enyl]-di-tert-butylhydrazine dicarboxylate
CAS NO:1026988-66-8
Molecular Formula:
Molecular Weight: 422.497
EINECS: N/A
Product Categories: N/A
Mol File: 1026988-66-8.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: trans-N,N'-[2-(4'-fluoro-2'-methoxyphenyl)-cyclopent-3-enyl]-di-tert-butylhydrazine dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: trans-N,N'-[2-(4'-fluoro-2'-methoxyphenyl)-cyclopent-3-enyl]-di-tert-butylhydrazine dicarboxylate(1026988-66-8)
EPA Substance Registry System: trans-N,N'-[2-(4'-fluoro-2'-methoxyphenyl)-cyclopent-3-enyl]-di-tert-butylhydrazine dicarboxylate(1026988-66-8)

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: 1026988-66-8(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

1026988-66-8 Suppliers

Recommended suppliersmore

1026988-66-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1026988-66-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,6,9,8 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1026988-66:
(9*1)+(8*0)+(7*2)+(6*6)+(5*9)+(4*8)+(3*8)+(2*6)+(1*6)=178
178 % 10 = 8
So 1026988-66-8 is a valid CAS Registry Number.

1026988-66-8Upstream product

179899-07-1 4-fluoro-2-methoxyphenylboronic acid

1026988-66-8Downstream Products

1026988-66-8Relevant articles and documents

Chemodivergence in enantioselective desymmetrization of diazabicycles: Ring-opening versus reductive arylation

Menard, Frederic,Lautens, Mark

, p. 2085 - 2088 (2008)

(Chemical Equation Presented) Divergent bicycle paths: A chemodivergent desymmetrization occurs after an initial enantioselective carbometalation step. The reaction brings a solution to the challenging problem of the enantioselective ring-opening of diazabicyclo-[2.2.1]heptanes to obtain arylated cyclopentenamines (see scheme, right). An alternative reaction pathway was discovered in which C-H insertion/1,4-metal migration occurs to give reductive arylation products (left).

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 1026988-66-8