基本情報
- CAS
30354-18-8- 標準SMILES
C=[N+](C)C.[Cl-]- InChIKey
ZJTROANVDZIEGB-UHFFFAOYSA-M- 分子式
- C3H8ClN
- 平均分子量
- 93.55 g/mol
名称と識別子
- 優先名称
- Dimethylmethylenammonium chloride
- IUPAC
- dimethyl(methylidene)azanium chloride
- 現地名
- N-メチル-N-メチレンメタンアミニウム·クロリド
- 英語名
- Eschenmoser's salt
- 分子式
- C3H8ClN
- 分子量
- 93.56
名称と別名
名称をさらに表示
データベース識別子
- CAS
30354-18-8- PubChem CID
- 11051579
- DTXSID
DTXSID60952697- EC Number
- 250-142-4
物性
構造計算による物性
- 極性表面積
- 3 Ų
- 水素結合供与体数
- 0
- 水素結合受容体数
- 1
- 回転可能結合数
- 0
- 重原子数
- 5
- 形式電荷
- 0
- 複雑度
- 26.3
物理化学的性質
- 融点
- 146 · 146-148 °C(lit.)
- 闪点
- 180 °F · 180 °F
- 貯蔵温度
- 30 °C · Store below +30°C.
- 溶解性
- Chloroform (Very Slightly, Heated), DMSO (Sparingly, Heated, Sonicated)
- 外見
- Solid
- 色
- White to Off-White
- BRN
- 505955 · 505955
- 安定性
- Hygroscopic, Unstable in Protic Solvent
- InChI
- 1S/C3H8N.ClH/c1-4(2)3;/h1H2,2-3H3;1H/q+1;/p-1
- InChIKey
- ZJTROANVDZIEGB-UHFFFAOYSA-M
- SMILES
- [Cl-].C[N+](C)=C
安全と法規制
GHS分類
GHS Classification
Danger
H228 (100%): Flammable solid [Danger Flammable solids]
P210, P240, P241, P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P370+P378, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 39 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
危険有害性情報
安全データ
- F
- 3-10-21
- wgk
- 3
- ridadr
- UN 1325 4.1/PG 3
- risk_code
- 36/37/38
- hazard_code
- Xi
- safety_code
- 26-36
- Hazard Classifications
- Eye Irrit. 2Flam. Sol. 2Skin Irrit. 2STOT SE 3
- ストレージクラス
- 4.1B - Flammable solid hazardous materials
化学と産業
応用分野
使用N,N-Dimethylmethyleneiminium chloride (Bhme′s salt) is a dimethylaminomethylating agent that can be used as one of the key reagents in the following applications:Electrophilic aminomethylation of aldehydes and ketones to synthesize corresponding Mannich products, also known as Mannich reaction.Preparation of dihydronaphthyridinones as HIV-1 integrase inhibitors.Preparation of cyanotetrahydrooxo-β-carbolines via cyclocondensation of cyanomethyl indole-2-carboxylate with ammonia.Asymmetric synthesis of phalarine via stereospecific Pictet-Spengler cyclocondensation and traceless chirality transfer from L-tryptophan.Synthesis of functionalized diarylpyrrolizines as inhibitors of microsomal prostaglandin E2 synthase-1 (mPGES-1) and 5-lipoxygenase (5-LOX).Synthesis of (±)-phalarine with the rearrangement of an azaspiroindolenine and Gassman oxindole preparation as key steps.
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