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4-Nitro-N-(1H-tetrazol-5-yl)benzamide is a chemical compound with the molecular formula C8H7N5O3. It is a derivative of benzamide, featuring a nitro group at the 4-position and a tetrazol-5-yl group attached to the nitrogen atom. 4-Nitro-N-(1H-tetrazol-5-yl)benzamide is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds. It is characterized by its yellow crystalline appearance and is typically used in research and development settings due to its reactivity and the ability to form various derivatives. The compound's properties, such as its solubility and stability, make it a valuable intermediate in the preparation of more complex molecules.

6229-22-7

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6229-22-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6229-22-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,2 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6229-22:
(6*6)+(5*2)+(4*2)+(3*9)+(2*2)+(1*2)=87
87 % 10 = 7
So 6229-22-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H6N6O3/c15-7(9-8-10-12-13-11-8)5-1-3-6(4-2-5)14(16)17/h1-4H,(H2,9,10,11,12,13,15)

6229-22-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-nitro-N-(2H-tetrazol-5-yl)benzamide

1.2 Other means of identification

Product number -
Other names Benzamide,4-nitro-N-(1H-tetrazol-5-yl)

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:6229-22-7 SDS

6229-22-7Downstream Products

6229-22-7Relevant academic research and scientific papers

From achiral tetrazolate-based tectons to chiral coordination networks: Effects of substituents on the structures and NLO properties

Liao, Jian-Zhen,Chen, Da-Chi,Li, Fang,Chen, Yong,Zhuang, Nai-Feng,Lin, Mei-Jin,Huang, Chang-Cang

, p. 8180 - 8185 (2013)

Using a hydrothermal synthesis method, the combination of four tetrazolate-yl acylamide tectons bearing substituents of different sizes, 4-nitro-N-(1H-tetrazol-5-yl)benzamide (H-NTBAN), 4-fluoro-N-(1H-tetrazol-5-yl) benzamide (H-NTBAF), N-(1H-tetrazol-5-yl)isonicotinamide (H-NTINA) and N-(1H-tetrazol-5-yl)thiophene-2-carboxamide (H-NTTCA), with cadmium dichloride led to four crystalline coordination networks, named Cd3(NTBAN) 6 (1), Cd(NTBAF)2 (2), Cd(NTINA)2 (3) and Cd(NTTCA)2 (4), respectively. The X-ray diffraction analysis revealed that compounds 2, 3 and 4 possess a 3D non-interpenetrated diamondoid framework, while compound 1 is of a 0D trinuclear structure. Wherein, compounds 2, 3 and 4 crystallized in chiral space groups with significant second harmonic generation (SHG) efficiencies. The effects of substituents in the semirigid tetrazole-yl acylamide tectons on the structural topologies as well as on the nonlinear optical properties of the generated coordination networks are discussed.

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