251569
1,3-Dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone
98%, for peptide synthesis
동의어(들):
1,3-Dimethyl-2-oxohexahydropyrimidine, N,N′-Dimethylpropylene urea, DMPU
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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
제품명
1,3-Dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone, 98%
Quality Level
분석
98%
양식
liquid
refractive index
n20/D 1.488 (lit.)
bp
146 °C/44 mmHg (lit.)
density
1.06 g/mL at 25 °C (lit.)
응용 분야
peptide synthesis
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
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애플리케이션
1,3-Dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone (DMPU) can be used:
DMPU/HF can be used as a nucleophilic fluorinating agent in fluoro-Prins reaction for the synthesis of substituted 4-fluorotetrahydropyrans and 4-fluoropiperidines.
- As a versatile solvent in N-alkylation of amines
- O-alkylation of aldoses , and in the synthesis of poly(aryl ethers).
- As urea solvent in the synthesis of 1-aryl-3,4,5-substituted pyrazoles by cyclocondensation of arylhydrazine hydrochlorides with 1,3-diketones.
- As an additive in asymmetric cyanoamidation.
DMPU/HF can be used as a nucleophilic fluorinating agent in fluoro-Prins reaction for the synthesis of substituted 4-fluorotetrahydropyrans and 4-fluoropiperidines.
Versatile solvent employed in N-alkylation of chiral, primary amines, O-alkylation of aldoses, and in the synthesis of poly(aryl ethers).
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
이미 열람한 고객
Intermolecular N-alkylation of amines under conditions of the Mitsunobu reaction: a new solid-phase synthesis of tertiary benzylamines
Zaragoza, Florencio and Stephensen, Henrik
Tetrahedron Letters, 41(11), 1841-1844 (2000)
Preparation of Fluorinated Tetrahydropyrans and Piperidines using a New Nucleophilic Fluorination Reagent DMPU/HF
Okoromoba OE, et al.
Organic Letters, 17(16), 3975-3977 (2015)
Thianthrene as an activating group for the synthesis of poly (aryl ether thianthrene)s by nucleophilic aromatic substitution
Edson JB and Knauss DM
Journal of Polymer Science Part A: Polymer Chemistry, 42(24), 6353-6363 (2004)
Synthesis, 1243-1243 (1993)
Highly Enantioselective Intramolecular Cyanoamidation:(+)-Horsfiline,(-)-Coerulescine, and (-)-Esermethole
Reddy VJ and Douglas CJ
Organic Letters, 12(5), 952-955 (2010)
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