Cas 1401082-54-9,endo-2-[2-(2,4,5-trifluorobenzyl)-1,1-dioxo-2H-1,2-benzothiazin-4(3H)-ylidene]acetic acid methyl ester

1401082-54-9

Post Buying Request

Basic information

Product Name: endo-2-[2-(2,4,5-trifluorobenzyl)-1,1-dioxo-2H-1,2-benzothiazin-4(3H)-ylidene]acetic acid methyl ester
Synonyms: endo-2-[2-(2,4,5-trifluorobenzyl)-1,1-dioxo-2H-1,2-benzothiazin-4(3H)-ylidene]acetic acid methyl ester
CAS NO:1401082-54-9
Molecular Formula:
Molecular Weight: 397.375
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: endo-2-[2-(2,4,5-trifluorobenzyl)-1,1-dioxo-2H-1,2-benzothiazin-4(3H)-ylidene]acetic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: endo-2-[2-(2,4,5-trifluorobenzyl)-1,1-dioxo-2H-1,2-benzothiazin-4(3H)-ylidene]acetic acid methyl ester(1401082-54-9)
EPA Substance Registry System: endo-2-[2-(2,4,5-trifluorobenzyl)-1,1-dioxo-2H-1,2-benzothiazin-4(3H)-ylidene]acetic acid methyl ester(1401082-54-9)

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: 1401082-54-9(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

1401082-54-9 Suppliers

Recommended suppliers

1401082-54-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1401082-54-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,1,0,8 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1401082-54:
(9*1)+(8*4)+(7*0)+(6*1)+(5*0)+(4*8)+(3*2)+(2*5)+(1*4)=99
99 % 10 = 9
So 1401082-54-9 is a valid CAS Registry Number.

1401082-54-9Upstream product

1349170-98-4 2-(2,4,5-trifluorobenzyl)-2H-1,2-benzothiazin-4(3H)-one 1,1-dioxide

1401082-54-9Downstream Products

1401082-53-8 endo-2-[2-(2,4,5-trifluorobenzyl)-1,1-dioxo-2H-1,2-benzothiazin-4(3H)-ylidene]acetic acid

1401082-54-9Relevant academic research and scientific papers

Selective synthesis and comparative activity of olefinic isomers of 1,2-benzothiazine-1,1-dioxide carboxylates as aldose reductase inhibitors

Parveen, Shagufta,Hussain, Saghir,Zhu, Shaojuan,Qin, Xiangyu,Hao, Xin,Zhang, Shuzhen,Lu, Jianglu,Zhu, Changjin

, p. 21134 - 21140 (2014/06/09)

α,β- and β,γ-unsaturated carboxylate isomers of 1,2-benzothiazine-1,1-dioxide were selectively synthesized via the Wittig olefination reaction under various temperature conditions. At 40 °C, α,β-unsaturated esters with high Z-stereoselectivity (83-87%) we

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 1401082-54-9