Cas 177493-79-7,Cyclohexanecarboxaldehyde, 2-(1-propenyl)-, [1alpha,2beta(E)]- (9CI)

177493-79-7

Post Buying Request

Basic information

Product Name: Cyclohexanecarboxaldehyde, 2-(1-propenyl)-, [1alpha,2beta(E)]- (9CI)
Synonyms: Cyclohexanecarboxaldehyde, 2-(1-propenyl)-, [1alpha,2beta(E)]- (9CI)
CAS NO:177493-79-7
Molecular Formula: C10H16O
Molecular Weight: 152.23344
EINECS: N/A
Product Categories: ALDEHYDE
Mol File: 177493-79-7.mol
Article Data: 2

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Cyclohexanecarboxaldehyde, 2-(1-propenyl)-, [1alpha,2beta(E)]- (9CI)(CAS DataBase Reference)
NIST Chemistry Reference: Cyclohexanecarboxaldehyde, 2-(1-propenyl)-, [1alpha,2beta(E)]- (9CI)(177493-79-7)
EPA Substance Registry System: Cyclohexanecarboxaldehyde, 2-(1-propenyl)-, [1alpha,2beta(E)]- (9CI)(177493-79-7)

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: 177493-79-7(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

177493-79-7 Suppliers

Recommended suppliersmore

177493-79-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 177493-79-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,4,9 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 177493-79:
(8*1)+(7*7)+(6*7)+(5*4)+(4*9)+(3*3)+(2*7)+(1*9)=187
187 % 10 = 7
So 177493-79-7 is a valid CAS Registry Number.

177493-79-7Upstream product

21661-97-2 (Z)-dec-7-enal

177493-79-7Downstream Products

177493-79-7Relevant articles and documents

Enantioselective organocatalytic singly occupied molecular orbital activation: The enantioselective α-enolation of aldehydes

Jang, Hye-Young,Hong, Jun-Bae,MacMillan, David W. C.

, p. 7004 - 7005 (2007)

The first enantioselective organocatalytic ∞-enolation of aldehydes has been accomplished using singly occupied molecular orbital (SOMO) catalysis. Chiral secondary amines react with aldehydes to form transient enamines that undergo selective one-electron

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 177493-79-7