41661
1,3-Dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone
absolute, over molecular sieve (H2O ≤0.05%), ≥99.0% (GC)
동의어(들):
1,3-Dimethyl-2-oxohexahydropyrimidine, N,N′-Dimethylpropylene urea, DMPU
로그인조직 및 계약 가격 보기
모든 사진(1)
About This Item
실험식(Hill 표기법):
C6H12N2O
CAS Number:
Molecular Weight:
128.17
Beilstein:
110562
EC Number:
MDL number:
UNSPSC 코드:
12352115
PubChem Substance ID:
NACRES:
NA.22
추천 제품
grade
absolute
Quality Level
분석
≥99.0% (GC)
양식
liquid
품질
over molecular sieve (H2O ≤0.05%)
refractive index
n20/D 1.488 (lit.)
n20/D 1.489
bp
146 °C/44 mmHg (lit.)
density
1.06 g/mL at 25 °C (lit.)
SMILES string
CN1CCCN(C)C1=O
InChI
1S/C6H12N2O/c1-7-4-3-5-8(2)6(7)9/h3-5H2,1-2H3
InChI key
GUVUOGQBMYCBQP-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
1,3-Dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone (DMPU) can be used as a:
- Solvent in the synthesis of 1-aryl-3,4,5-substituted pyrazoles by cyclocondensation of 1,3-diketones with arylhydrazine hydrochlorides.
- Chelating solvent in the trifluoromethylation of activated and non-activated halogenated double bonds.
- Ligand in ortho-alkylation of secondary benzamide catalyzed by cobalt.
기타 정보
Aprotic, dipolar solvent, which is an excellent replacement of the carcinogenic HMPA as cosolvent for highly reactive nucleophiles and bases. High Z-selectivity in enolate formation; DMPU was shown to be non-mutagenic and safe.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Repr. 2
Storage Class Code
10 - Combustible liquids
WGK
WGK 1
Flash Point (°F)
249.8 °F - closed cup
Flash Point (°C)
121 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
가장 최신 버전 중 하나를 선택하세요:
시험 성적서(COA)
Lot/Batch Number
이미 열람한 고객
Efficient Trifluoromethylation of Activated and Non-Activated Alkenyl Halides by Using (Trifluoromethyl) trimethylsilane.
Hafner A and Braese S
Advanced Synthesis & Catalysis, 353(16), 3044-3048 (2011)
anon.
Chimia, 39, 147-147 (1985)
Cobalt-catalyzed ortho-alkylation of secondary benzamide with alkyl chloride through directed C- H bond activation.
Chen Q, et al.
Journal of the American Chemical Society, 133(3), 428-429 (2010)
R.E. Ireland et al.
The Journal of Organic Chemistry, 56, 650-650 (1991)
Efficient Trifluoromethylation of Activated and Non-Activated Alkenyl Halides by Using (Trifluoromethyl) trimethylsilane.
Hafner A and Braese S
advanced synthesis and catalysis, 353(16), 3044-3048 (2011)
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