92457
三亚甲基亚胺
purum, ≥97.0% (GC)
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关于此项目
经验公式（希尔记法）:
C3H7N
化学文摘社编号:
分子量:
57.09
EC Number:
207-963-8
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
102384
MDL number:
grade
purum
assay
≥97.0% (GC)
refractive index
n20/D 1.431, n20/D 1.432 (lit.)
bp
61-62 °C (lit.)
density
0.847 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
C1CNC1
InChI
1S/C3H7N/c1-2-4-3-1/h4H,1-3H2
InChI key
HONIICLYMWZJFZ-UHFFFAOYSA-N
signalword
Danger
hcodes
Hazard Classifications
Flam. Liq. 2 - Skin Corr. 1B
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
-5.8 °F - closed cup
flash_point_c
-21 °C - closed cup
ppe
Faceshields, Gloves, Goggles
法规信息
新产品
此项目有
Michael J Brown et al.
Organic letters, 13(7), 1686-1689 (2011-03-04)
An efficient two-step synthesis of a wide range of 3-methylene-1,2-diazetidines has been developed through application of a Cu(I)-catalyzed 4-exo ring closure. The double bond of this new class of strained heterocycle can be functionalized in a stereocontrolled manner by using
Asta Žukauskaitė et al.
Amino acids, 41(3), 541-558 (2011-03-23)
A short synthesis of alkyl 2-(bromomethyl)aziridine-2-carboxylates and alkyl 3-bromoazetidine-3-carboxylates was developed involving amination, bromination, and base-induced cyclization of alkyl 2-(bromomethyl)acrylates. The aziridines are the kinetically favored cyclization products and could be transformed into 3-bromoazetidine-3-carboxylic acid derivatives via thermal isomerization. The
Gert Callebaut et al.
Organic & biomolecular chemistry, 10(11), 2326-2338 (2012-02-09)
The efficient asymmetric synthesis of new chiral γ-chloro-α,β-diamino acid derivatives via highly diastereoselective Mannich-type reactions of N-(diphenylmethylene) glycine esters across a chiral α-chloro-N-p-toluenesulfinylimine was developed. The influence of the base, LDA or LiHMDS, used for the formation of the glycine
Marco Caricato et al.
The Journal of chemical physics, 133(5), 054104-054104 (2010-08-17)
We investigate how the choice of the link atom bond length affects an electronic transition energy calculation with the so-called our own N-layer integrated molecular orbital molecular mechanics (ONIOM) hybrid method. This follows our previous paper [M. Caricato et al.
Stephen D Roughley et al.
Bioorganic & medicinal chemistry letters, 22(2), 901-906 (2012-01-03)
We describe here our attempts to optimise the human fatty acid amide hydrolase (FAAH) inhibition and physicochemical properties of our previously reported tetrasubstituted azetidine urea FAAH inhibitor, VER-156084. We describe the SAR of a series of analogues and conclude with
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