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N,N-Dimethylmethyleneiminium chloride_Molecular_structure_CAS_30354-18-8)
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N,N-Dimethylmethyleneiminium chloride

Catalog No. 483893 Name Sigma Aldrich
CAS Number 30354-18-8 Website http://www.sigmaaldrich.com
M. F. C3H8ClN Telephone 1-800-521-8956
M. W. 93.55532 Fax
Purity 90% Email
Storage Chembase ID: 139989

SYNONYMS

Title
N,N-二甲基氯烯亚胺
IUPAC name
dimethyl(methylidene)azanium chloride
IUPAC Traditional name
dimethyl(methylidene)azanium chloride
Synonyms
Eschenmoser 盐
Eschenmoser’s salt
Methylenedimethylammonium chloride
Dimethylformiminium chloride

DATABASE IDS

EC Number 250-142-4
PubChem SID 24871926
CAS Number 30354-18-8
Beilstein Number 505955
MDL Number MFCD00011809

PROPERTIES

Grade technical grade
Linear Formula CH2=N+(CH3)2Cl-
Purity 90%
Flash Point 82 °C
Flash Point 179.6 °F
Melting Point 146-148 °C(lit.)
GHS Pictograms GHS02
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H228-H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P210-P261-P305 + P351 + P338
RID/ADR UN 1325 4.1/PG 3
Risk Statements 36/37/38
Safety Statements 26-36
Hazard Class 4.1
UN Number 1325
Packing Group 3
German water hazard class 3

DETAILS

Description (English)
Packaging
5, 25 g in glass bottle
Application
Reacant for:Preparation of dihydronaphthyridinones as HIV-1 integrase inhibitors1Mannich reactions2Preparation of cyanotetrahydrooxo-β-carbolines via cyclocondensation reactions3Asymmetric synthesis of phalarine via stereospecific Pictet-Spengler cyclocondensation and traceless chirality transfer from L-tryptophan4Synthesis of functionalized diarylpyrrolizines as inhibitors of microsomal prostaglandin E2 synthase-1 (mPGES-1) and 5-lipoxygenase (5-LOX)5Synthesis of (±)-phalarine with the rearrangement of an azaspiroindolenine and Gassman oxindole preparation as key steps6
Description (简体中文)
包装
5, 25 g in glass bottle
Application
Reacant for:Preparation of dihydronaphthyridinones as HIV-1 integrase inhibitors1Mannich reactions2Preparation of cyanotetrahydrooxo-β-carbolines via cyclocondensation reactions3Asymmetric synthesis of phalarine via stereospecific Pictet-Spengler cyclocondensation and traceless chirality transfer from L-tryptophan4Synthesis of functionalized diarylpyrrolizines as inhibitors of microsomal prostaglandin E2 synthase-1 (mPGES-1) and 5-lipoxygenase (5-LOX)5Synthesis of (±)-phalarine with the rearrangement of an azaspiroindolenine and Gassman oxindole preparation as key steps6

REFERENCES