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Bicyclo[2.2.1]hept-5-ene-2-sulfonamide (9CI) is a chemical compound with the molecular formula C7H11NO2S. It is a derivative of bicyclo[2.2.1]hept-5-ene, a bicyclic hydrocarbon, with a sulfonamide group attached to the 2-position. Bicyclo[2.2.1]hept-5-ene-2-sulfonamide (9CI) is characterized by its unique bicyclic structure and the presence of a sulfonamide functional group, which can form hydrogen bonds and has potential applications in the synthesis of various pharmaceuticals and agrochemicals. The compound's properties, such as solubility, stability, and reactivity, can be influenced by the presence of the sulfonamide group, making it an interesting target for further chemical modifications and studies.

7167-08-0

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7167-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7167-08-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,6 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7167-08:
(6*7)+(5*1)+(4*6)+(3*7)+(2*0)+(1*8)=100
100 % 10 = 0
So 7167-08-0 is a valid CAS Registry Number.
InChI:InChI=1/C20H20F2N4O2S/c1-12-4-5-13(2)17(8-12)28-11-15-9-14(6-7-16(15)27-3)10-23-26-19(18(21)22)24-25-20(26)29/h4-10,18H,11H2,1-3H3,(H,25,29)

7167-08-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name bicyclo[2.2.1]hept-2-ene-5-sulfonamide

1.2 Other means of identification

Product number -
Other names BICYCLO[2.2.1]HEPT-5-ENE-2-SULFONAMIDE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7167-08-0 SDS

7167-08-0Upstream product

7167-08-0Downstream Products

7167-08-0Relevant academic research and scientific papers

Metal-free intramolecular aziridination of alkenes using hypervalent iodine based sulfonyliminoiodanes

Moriarty, Robert M.,Tyagi, Sachin

supporting information; experimental part, p. 364 - 366 (2010/03/24)

(Figure presented) Intramolecular aziridination of alkenyl sulfonyliminoiodanes occurs thermally In the absence of conventional metal catalysts such as Rh(II) and Cu(II). In rigid molecular systems, conversions are near quantitative. The scope of the nonm

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