317276
Chloroacetaldehyde solution
~55 wt. % in H2O
동의어(들):
α-Chloroacetaldehyde, 2-Chloro-1-ethanal, 2-Chloroacetaldehyde, 2-Chloroethanal, Monochloroacetaldehyde
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모든 사진(1)
About This Item
Linear Formula:
ClCH2CHO
CAS Number:
Molecular Weight:
78.50
Beilstein:
1071226
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
양식
liquid
Quality Level
농도
~55 wt. % in H2O
refractive index
n20/D 1.4036
density
1.236 g/mL at 25 °C
작용기
aldehyde
chloro
SMILES string
[H]C(=O)CCl
InChI
1S/C2H3ClO/c3-1-2-4/h2H,1H2
InChI key
QSKPIOLLBIHNAC-UHFFFAOYSA-N
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애플리케이션
Chloroacetaldehyde solution can be used for the synthesis of:
- Etheno derivatives of nucleotides.
- 2,3-Disubstituted pyrroles by Hantzsch reaction.
- Aminotetrahydronaphthalene ketopiperazine scaffolds as potent MCH-R1 antagonists.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 1 Inhalation - Acute Tox. 2 Dermal - Acute Tox. 3 Oral - Aquatic Acute 1 - Carc. 2 - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
Flash Point (°F)
143.6 °F - closed cup
Flash Point (°C)
62 °C - closed cup
개인 보호 장비
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
이미 열람한 고객
Determination of leukocyte DNA 6-thioguanine nucleotide levels by high-performance liquid chromatography with fluorescence detection
Olesen KM, et al.
Journal of Chromatography. B, Biomedical Applications, 864(1-2), 149-155 (2008)
The efficacy and cardiac evaluation of aminomethyl tetrahydronaphthalene ketopiperazines: a novel class of potent MCH-R1 antagonists
Mendez-Andino JL, et al.
Bioorganic & Medicinal Chemistry, 15(5), 2092-2105 (2007)
Novel synthesis of [13C4, 15N] 1H-pyrrole-2, 3, 5-tricarboxylic acid: an important biomarker for melatonin metabolism
Skaddan MB
Journal of Labelled Compounds & Radiopharmaceuticals, 53(2), 73-77 (2010)
V Nagarajavel et al.
The Journal of biological chemistry, 282(32), 23622-23630 (2007-06-16)
H-NS inhibits transcription by forming repressing nucleoprotein complexes next to promoters. We investigated repression by binding of H-NS within the transcription unit using the bgl and proU operons. Repression of both operons requires a downstream regulatory element (DRE) in addition
Zeinab Yaseen et al.
Archives of toxicology, 82(9), 607-614 (2008-01-25)
The Fanconi syndrome is a common side effect of the chemotherapeutic agent ifosfamide. Current evidences suggest that chloroacetaldehyde (CAA), one of the main metabolites of ifosfamide activation, contributes to its nephrotoxicity. However, the pathophysiology of CAA-induced Fanconi syndrome is not
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