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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%

别名:

(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

线性分子式:

CH₃CH(NH₂)CH₂NH₂·2HCl

CAS号:

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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412554

(R)-(+)-二氨基丙烷二盐酸盐

Sigma-Aldrich

117498

1,2-二氨基丙烷

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D23602

1,3-二氨基丙烷

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D13208

1,4-二氨基丁烷

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226920

2,2-二甲基-1,3-丙二胺

Sigma-Aldrich

726664

(R)-1-(4-甲基苯基)乙胺

Sigma-Aldrich

701408

1,2-二氨基(丙烷-d₆)

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

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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

Hsu FL, et al.

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

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

Miller DD, et al.

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

Synthesis and in vivo evaluation of cyclic diaminopropane BACE-1 inhibitors.

Lorin A Thompson et al.

Bioorganic & medicinal chemistry letters, 21(22), 6909-6915 (2011-10-07)

The synthesis, evaluation, and structure-activity relationships of a set of related constrained diaminopropane inhibitors of BACE-1 are described. The full in vivo profile of an optimized inhibitor in both normal and P-gp deficient mice is compared with data generated in

Distribution of diaminopropane, putrescine and cadaverine in Haemophilus and Actinobacillus.

K Hamana et al.

Microbios, 103(404), 43-51 (2000-10-18)

Cellular levels of diaminopropane, putrescine and cadaverine, and decarboxylase activities to produce these diamines in six species (16 strains) of Haemophilus and four species (5 strains) of Actinobacillus belonging to the family Pasteurellaceae of the gamma subclass of the class

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