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60023-35-0

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60023-35-0 Usage

General Description

Pyrazine, (bromomethyl)- (9CI) is a chemical compound with the formula C4H4BrN2. It belongs to the family of pyrazine compounds, which are heterocyclic aromatic compounds containing a six-membered ring with two nitrogen atoms at opposite positions. The bromomethyl group in the compound indicates the presence of a bromine atom attached to a methylene group. Pyrazine, (bromomethyl)- (9CI) has potential applications in organic synthesis, pharmaceuticals, and agrochemicals. Its molecular structure and reactivity make it useful in the production of various fine chemicals and medicinal compounds. Pyrazine, (bromomethyl)- (9CI) is characterized by its strong odor and is considered a hazardous chemical that requires safe handling and storage practices.

Check Digit Verification of cas no

The CAS Registry Mumber 60023-35-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,0,2 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 60023-35:
(7*6)+(6*0)+(5*0)+(4*2)+(3*3)+(2*3)+(1*5)=70
70 % 10 = 0
So 60023-35-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H5BrN2/c6-3-5-4-7-1-2-8-5/h1-2,4H,3H2

60023-35-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(Bromomethyl)pyrazine

1.2 Other means of identification

Product number -
Other names 2-(bromomethyl)pyrazine

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:60023-35-0 SDS

60023-35-0Relevant articles and documents

Nonameric porphyrin assemblies - Formation and intra-assembly energy transfer reactions

Sasaki, Ken,Sugou, Kenji,Miyamoto, Koji,Hirai, Jyun-Ichi,Tsubouchi, Shigetaka,Miyasaka, Hiroshi,Itaya, Akira,Kuroda, Yasuhisa

, p. 2852 - 2860 (2004)

The nonameric porphyrin assemblies constructed with the series of free base tetraphenylporphyrins Pn having four pyrazine moieties linked with alkyl chains of different lengths, (CH2)n (n- 1, 5, 9, 17, 30), and dimeric [mesotetrakis(2-carboxy-4-nonylphenyl)porphyrinato]zinc(II), ZnP2, show the effective light-collection effect and the typical Foerster-type energy transfer from ZnP2 to Pn.

Inhibition of the Cysteine Protease Human Cathepsin L by Triazine Nitriles: Amide???Heteroarene π-Stacking Interactions and Chalcogen Bonding in the S3 Pocket

Giroud, Maude,Ivkovic, Jakov,Martignoni, Mara,Fleuti, Marianne,Trapp, Nils,Haap, Wolfgang,Kuglstatter, Andreas,Benz, J?rg,Kuhn, Bernd,Schirmeister, Tanja,Diederich, Fran?ois

supporting information, p. 257 - 270 (2017/02/15)

We report an extensive “heteroarene scan” of triazine nitrile ligands of the cysteine protease human cathepsin L (hCatL) to investigate π-stacking on the peptide amide bond Gly67–Gly68 at the entrance of the S3 pocket. This heteroarene???peptide bond stacking was supported by a co-crystal structure of an imidazopyridine ligand with hCatL. Inhibitory constants (Ki) are strongly influenced by the diverse nature of the heterocycles and specific interactions with the local environment of the S3 pocket. Binding affinities vary by three orders of magnitude. All heteroaromatic ligands feature enhanced binding by comparison with hydrocarbon analogues. Predicted energetic contributions from the orientation of the local dipole moments of heteroarene and peptide bond could not be confirmed. Binding of benzothienyl (Ki=4 nm) and benzothiazolyl (Ki=17 nm) ligands was enhanced by intermolecular C?S???O=C interactions (chalcogen bonding) with the backbone C=O of Asn66 in the S3 pocket. The ligands were also tested for the related enzyme rhodesain.

NEW COMPOUNDS

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Page 62-63, (2010/02/06)

The present invention relates to new compounds of formula I, wherein P Q X1 X2 X3 X4 X5 R R1 R2 R3 R4R5 G M1 M2 M3 m and n are defined as in formula I, a process for their preparation and new intermediates prepared therein, pharmaceutical formulations containing said compounds and to the use of said compounds in therapy.

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