추천 제품
분석
≥98%
형태
powder or crystals
bp
225-230 °C/15 mmHg (lit.)
mp
231-233 °C (lit.)
solubility
H2O: 1 g in 10 mL, clear, colorless
SMILES string
Cl[H].CN
InChI
1S/CH5N.ClH/c1-2;/h2H2,1H3;1H
InChI key
NQMRYBIKMRVZLB-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
Methylamine hydrochloride is used as a buildingblock for the synthesis of various organic compounds.
애플리케이션
Methylamine hydrochloride can be used as a reactant to synthesize:
- Betahistine via aza-Michael reaction with 2-vinylpyridine in water.
- Azatripyrrolic and azatetrapyrrolic macrocycles by reacting with pyrrole and formaldehyde via base-catalyzed Mannich reaction.
- Tetrahydropyridines via Aza-Diels–Alder reaction with dienes and aldehydes.
- N-methylsecondary arylamines from aryl chlorides via nickel-catalyzed amination reaction.
신호어
Warning
유해 및 위험 성명서
예방조치 성명서
Hazard Classifications
Acute Tox. 4 Oral
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point (°F)
408.7 °F - closed cup
Flash Point (°C)
209.3 °C - closed cup
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
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Ammoniomethyl trifluoroborates are very powerful reagents that can be used to access biologically relevant aryl- and heteroaryl-methylamine motifs via Suzuki-Miyaura cross-couplings. Until now, this method was limited to the production of tertiary and primary amines. The synthesis of a large
Journal of the American Chemical Society, 134(15), 6540-6543 (2012-04-06)
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