280909
(Chloromethylene)dimethyliminium chloride
95%
동의어(들):
(Chlormethylene)dimethylammonium chloride, Arnold′s reagent, Dimethylchloroformiminium chloride, Vilsmeier reagent
로그인조직 및 계약 가격 보기
모든 사진(1)
About This Item
Linear Formula:
ClCH=N(CH3)2Cl
CAS Number:
Molecular Weight:
128.00
Beilstein:
3566322
EC Number:
MDL number:
UNSPSC 코드:
12352101
PubChem Substance ID:
NACRES:
NA.22
추천 제품
Quality Level
분석
95%
양식
solid
반응 적합성
reaction type: C-C Bond Formation
불순물
<5% DMF
mp
132 °C (dec.) (lit.)
작용기
amine
chloro
저장 온도
2-8°C
SMILES string
[Cl-].C\[N+](C)=C\Cl
InChI
1S/C3H7ClN.ClH/c1-5(2)3-4;/h3H,1-2H3;1H/q+1;/p-1
InChI key
QQVDYSUDFZZPSU-UHFFFAOYSA-M
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
Reagent or Reactant for the synthesis of:
Used for studying organic photosensitizers for application in dye-sensitized solar cells
- β-Lactams vis the Staudinger reaction
- N-vinyl substituted indoles via cross coupling of NH-indoles with vinyl bromides
- Multi ring-fused 2-pyridone-based fluorescent scaffold
- ester prodrugs as anti-poxvirus agents
- Trimethine cyanine dyes for sensing G-quadruplex formation
- Phospha-isosteres via Hundsdiecker-Barton iododecacarboxylation
- 2-Azetidinones via [2+2]-cycloaddition
Used for studying organic photosensitizers for application in dye-sensitized solar cells
Reagent used to prepare ß-lactams from ß-amino acids via carboxyl activation and cyclodehydration. Also used to convert α-aminonitriles into 4-chloroimidazoles.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Repr. 1B - Skin Corr. 1A
보충제 위험성
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
가장 최신 버전 중 하나를 선택하세요:
이미 열람한 고객
J. Chem. Res. (M), 705-705 (2005)
Tetrahedron Letters, 47, 5451-5451 (2006)
Azhar Abbas et al.
Bioorganic chemistry, 82, 163-177 (2018-10-16)
Benzohydrazide derivatives 1-43 were synthesized via "one-pot" reaction and structural characterization of these synthetic derivatives was carried out by different spectroscopic techniques such as 1H NMR and EI-MS. The synthetic molecules were evaluated for their in vitro urease inhibitory activity.
Martin Mlateček et al.
Dalton transactions (Cambridge, England : 2003), 44(46), 20242-20253 (2015-11-06)
The reaction of PhBCl2 with 1H-1,2,4-λ(3)-diazaphosphole in the presence of NEt3 gives a new scorpionate ligand, phenyl-tris(1,2,4-diazaphospholyl)borate (PhTdap). The coordination behaviour of this ligand toward transition and non-transition metals has been comprehensively studied. In the thallium(I) complex, Tl(PhTdap), κ(2)-N,N bonding
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