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412562

(S)-(-)-二氨基丙烷二盐酸盐

Name: (<I>S</I>)-(-)-二氨基丙烷 二盐酸盐
Brand: ALDRICH

99%

同義詞:

(S)-(-)-丙二胺二盐酸盐, (S)-1,2-丙二胺二盐酸盐

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About This Item

線性公式:

CH₃CH(NH₂)CH₂NH₂·2HCl

CAS號碼:

19777-66-3

分子量：:

147.05

Beilstein:

5740936

MDL號碼:

MFCD00050706

分類程式碼代碼:

12352116

PubChem物質ID:

24865810

NACRES:

NA.22

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S55701

N,N'-BIS-TRITYL-PROPANE-1,3-DIAMINE

Sigma-Aldrich

T8656

硫脲

Sigma-Aldrich

736570

Acetoacetyl-¹³C₄ coenzyme A lithium salt hydrate

品質等級

100

化驗

99%

光學活性

[α]22/D −4°, c = 20 in H₂O

mp

227-229 °C (lit.)

官能基

amine

SMILES 字串

Cl.Cl.C[C@H](N)CN

InChI

1S/C3H10N2.2ClH/c1-3(5)2-4;;/h3H,2,4-5H2,1H3;2*1H/t3-;;/m0../s1

InChI 密鑰

AEIAMRMQKCPGJR-QTNFYWBSSA-N

應用

(S)-(-)-1,2-Diaminopropane dihydrochloride may be used in the preparation of following chiral imidazoline derivatives, which show moderate α-adrenergic blocking activity:

(S)-(-)-4-methyl-2-(1-naphthylmethyl)imidazoline hydrochloride[1]
(S)-(-)-2-benzyl-4-methylimidazoline picrate[2]
(S )-(-)-2-[(2,6-dichlorophenyl)imino]-4-methylimidazolidine hydrochloride[2]

象形圖

GHS07

訊號詞

Warning

危險聲明

H315,H319,H335

防範說明

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves

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分析證明 (COA)

Lot/Batch Number

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Stereochemical studies of adrenergic drugs. Optically active derivatives of imidazolines.

Miller DD, et al.

Journal of Medicinal Chemistry, 19(12), 1382-1384 (1976)

Optically active derivatives of imidazolines: a-Adrenergic blocking properties.

Hsu FL, et al.

Journal of Medicinal Chemistry, 23(11), 1232-1235 (1980)

Enrichment of trace amounts of copper(II) ions in water samples using octadecyl silica disks modified by a Schiff base ionophore prior to flame atomic absorption spectrometric determination.

S A M Fathi et al.

Journal of hazardous materials, 164(1), 133-137 (2008-09-10)

Bis(5-bromo-2-hydroxybenzaldehyde)-1,2-propanediimine is synthesized by the reaction of 5-bromo-2-hydroxybenzaldehyde and 1,2-diaminopropane in ethanol. This ligand is used as a modifier of octadecyl silica disks for preconcentration of trace amounts of copper(II) ions, followed by nitric acid elution and flame atomic absorption

Conformational change of spermidine upon interaction with adenosine triphosphate in aqueous solution.

Keisuke Maruyoshi et al.

Chemistry (Weinheim an der Bergstrasse, Germany), 15(7), 1618-1626 (2009-01-09)

Endogenous polyamines, represented by putrescine, spermidine, and spermine, are known to exert their physiological functions by interacting with polyanionic biomolecules such as DNA, RNA, adenosine triphosphate (ATP), and phospholipids. Very few examples of conformation analysis have been reported for these

Chiral cyanide-bridged Mn(II)Mn(III) ferrimagnets, [Mn(II)(HL)(H2O)][Mn(III)(CN)6].2H2O (L = S- or R-1,2-diaminopropane): syntheses, structures, and magnetic behaviors.

Wakako Kaneko et al.

Journal of the American Chemical Society, 129(2), 248-249 (2007-01-11)

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(S)-(-)-二氨基丙烷二盐酸盐