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Merck
모든 사진(2)

Key Documents

117501

Sigma-Aldrich

2,6-Dinitrobenzaldehyde

98%

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About This Item

Linear Formula:
(O2N)2C6H3CHO
CAS Number:
Molecular Weight:
196.12
Beilstein:
2113951
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

분석

98%

형태

solid

mp

120-122 °C (lit.)

작용기

aldehyde
nitro

저장 온도

2-8°C

SMILES string

[H]C(=O)c1c(cccc1[N+]([O-])=O)[N+]([O-])=O

InChI

1S/C7H4N2O5/c10-4-5-6(8(11)12)2-1-3-7(5)9(13)14/h1-4H

InChI key

WHFZQNNDIJKLIO-UHFFFAOYSA-N

유사한 제품을 찾으십니까? 방문 제품 비교 안내

일반 설명

2,6-Dinitrobenzaldehyde is the major intermediate formed by the combined ozonation of 2,6-dinitrotoluene with hydrogen peroxide and UV radiation.

애플리케이션

2,6-Dinitrobenzaldehyde was used in the synthesis of free base tetrakis(2,6-dinitrophenyl) porphyrin.

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

표적 기관

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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이 제품을 이미 가지고 계십니까?

문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Synthesis and spectroscopic characterization of bis-pocket porphyrins: tetrakis (2', 6'-dinitrophenyl) porphyrin and catalytic activity of a manganese (III) chloride derivative in alkane oxidation.
Quintana CA, et al.
Inorganic Chemistry, 28(18), 3421-3425 (1989)
Nitroaromatic hydrocarbon ozonation in water. 2. Combined ozonation with hydrogen peroxide or UV radiation.
Beltran FJ, et al
Industrial & Engineering Chemistry Research, 37(1), 32-40 (1998)
M Mori et al.
Xenobiotica; the fate of foreign compounds in biological systems, 19(7), 731-741 (1989-07-01)
1. Unchanged 2,6-dinitrotoluene (2,6-DNT), 2-amino-6-nitrotoluene, 2,6-dinitrobenzyl alcohol, 2-amino-6-nitrobenzyl alcohol, conjugated 2,6-dinitrobenzyl alcohol and conjugated 2-amino-6-nitrobenzyl alcohol were detected in urine of male Wistar rats dosed with 2,6-DNT. The major metabolite was conjugated 2,6-dinitrobenzyl alcohol, which accounted for about 1.5% of
M Sayama et al.
Mutation research, 243(1), 47-52 (1990-01-01)
The mutagenicities and theoretical reactivity indices of 2,4-dinitrobenzaldehyde (2,4-DNBAl) and 2,6-dinitrobenzaldehyde (2,6-DNBAl) were investigated using Salmonella typhimurium strains TA98, TA98NR, TA98/1,8-DNP6, and TA100, TA100NR and TA100/1,8-DNP6, by means of the modified intermediate neglect of differential overlap/3 (MINDO)/3) method. The mutagenic

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