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675605-72-8

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675605-72-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 675605-72-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,5,6,0 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 675605-72:
(8*6)+(7*7)+(6*5)+(5*6)+(4*0)+(3*5)+(2*7)+(1*2)=188
188 % 10 = 8
So 675605-72-8 is a valid CAS Registry Number.

675605-72-8SDS

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 1-(4-methanesulfonylphenyl)-5-(4-methylphenyl)-3-trifluoromethyl-1H-pyrazole

1.2 Other means of identification

Product number -
Other names celecoxib

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:675605-72-8 SDS

675605-72-8Relevant articles and documents

Primary Sulfonamide Functionalization via Sulfonyl Pyrroles: Seeing the N?Ts Bond in a Different Light

Ozaki, Tomoya,Yorimitsu, Hideki,Perry, Gregory J. P.

supporting information, p. 15387 - 15391 (2021/10/04)

Despite common occurrence in molecules of value, methods for transforming sulfonamides are distinctly lacking. Here we introduce easy-to-access sulfonyl pyrroles as synthetic linchpins for sulfonamide functionalization. The versatility of the sulfonyl pyrrole unit is shown by generating a variety of products through chemical, electrochemical and photochemical pathways. Preliminary results on the direct functionalization of primary sulfonamides are also provided, which may lead to new modes of activation.

Development of celecoxib-derived antifungals for crop protection

Liu, Xiuxiu,Ma, Yihui,Sun, Xianglong,Yang, Jun,Yang, Lirong

supporting information, (2020/02/27)

Selective COX-2 inhibitor celecoxib was found directly inhibiting the growth of tested phytopathogenic fungi with the inhibitory rate ranging from 30 to 40% at 100 μg/ml. Lead optimization of celecoxib led to the identification of compound 12 among its derivatives as the most active antifungal candidate. The antifungal effect of compound 12 was supposed to be independent of COX-2 inhibition. Transcriptome profiling analysis of Fusarium graminearium (PH-1) treated with compound 12 brought about 406 up-regulated and 572 down-regulated differentially express genes (DEGs) respectively.

Discovery of synthetic small molecules that enhance the number of stomata: C-H functionalization chemistry for plant biology

Ziadi, Asraa,Uchida, Naoyuki,Kato, Hiroe,Hisamatsu, Rina,Sato, Ayato,Hagihara, Shinya,Itami, Kenichiro,Torii, Keiko U.

, p. 9632 - 9635 (2017/09/01)

The increasing climate changes and global warming are leading to colossal agricultural problems such as abatement of food production and quality. As stomatal development is considered to play a key role in crop plant productivity and water-use efficiency,

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