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About This Item
Linear Formula:
HC≡CCH2NH2 · HCl
CAS Number:
Molecular Weight:
91.54
Beilstein:
3669858
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
95%
form
powder
reaction suitability
reaction type: click chemistry
mp
179-182 °C (lit.)
storage temp.
2-8°C
SMILES string
Cl.NCC#C
InChI
1S/C3H5N.ClH/c1-2-3-4;/h1H,3-4H2;1H
InChI key
IKXNIQJDNKPPCH-UHFFFAOYSA-N
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Related Categories
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Thomas Hermanns et al.
Life science alliance, 3(9) (2020-07-29)
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Adrian Sulistio et al.
Chemical communications (Cambridge, England), 47(4), 1151-1153 (2010-12-15)
Highly functionalized water soluble core cross-linked star (CCS) polymers having degradable cores and hierarchical functionalities spanning from the peripheral groups along the arms to the core have been synthesized entirely from amino acid building blocks. The core-isolated moieties were shown
Claudio Gnaccarini et al.
Organic & biomolecular chemistry, 10(27), 5258-5265 (2012-06-02)
Transglutaminases (TGases) catalyse the transamidation of glutamine residues with primary amines. Herein we report the first FRET-based activity assay for the direct detection of the ligation (transamidation) reaction mediated by tissue TGase (TG2). This novel assay was then used in
The marriage of organocatalysis with metal catalysis: access to multisubstituted chiral 2,5-dihydropyrroles by cascade iminium/enamine-metal cooperative catalysis.
Wangsheng Sun et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 17(50), 13958-13962 (2011-11-19)
Parminder Kaur et al.
Organic & biomolecular chemistry, 8(5), 1091-1096 (2010-02-19)
A variety of substituted chiral propargylamines have been synthesized by reacting chiral N-phosphonylimines with lithium aryl/alkyl acetylides. Seventeen examples were studied to give excellent yields (>90%) and diastereoselectivities (96 : 4 to 99 : 1). It was found that the
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