Cas 83241-54-7,Morpholine-4-carboximidothioic acid (Z)-3-(4-methoxy-phenyl)-3-oxo-propenyl ester; compound with perchloric acid

83241-54-7

Post Buying Request

Basic information

Product Name: Morpholine-4-carboximidothioic acid (Z)-3-(4-methoxy-phenyl)-3-oxo-propenyl ester; compound with perchloric acid
Synonyms: Morpholine-4-carboximidothioic acid (Z)-3-(4-methoxy-phenyl)-3-oxo-propenyl ester; compound with perchloric acid
CAS NO:83241-54-7
Molecular Formula:
Molecular Weight: 406.844
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: Morpholine-4-carboximidothioic acid (Z)-3-(4-methoxy-phenyl)-3-oxo-propenyl ester; compound with perchloric acid(CAS DataBase Reference)
NIST Chemistry Reference: Morpholine-4-carboximidothioic acid (Z)-3-(4-methoxy-phenyl)-3-oxo-propenyl ester; compound with perchloric acid(83241-54-7)
EPA Substance Registry System: Morpholine-4-carboximidothioic acid (Z)-3-(4-methoxy-phenyl)-3-oxo-propenyl ester; compound with perchloric acid(83241-54-7)

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: 83241-54-7(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

83241-54-7 Suppliers

Recommended suppliers

83241-54-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83241-54-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,2,4 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 83241-54:
(7*8)+(6*3)+(5*2)+(4*4)+(3*1)+(2*5)+(1*4)=117
117 % 10 = 7
So 83241-54-7 is a valid CAS Registry Number.

83241-54-7Upstream product

83241-54-7Downstream Products

83241-54-7Relevant academic research and scientific papers

KETOVINYLIERUNG VON THIOCARBONAMIDEN UND THIOHARNSTOFFEN. ZUR AMBIDENZ DER THIOAMIDFUNKTION

Spitzner, R.,Mielke, D.,Scholz, D.,Schroth, W.,Preiss, A.

, p. 927 - 936 (2007/10/02)

Thiocarbamides and thioureas 1 react as ambident systems with β-chlorovinyl ketones 2 to give the S--salts 3-5.Those obtained from monoprotic 1 undergo deprotonation, yielding isolable S-thioimidateesters or -isothioureas 6 r

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 83241-54-7