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Merck

C27409

Sigma-Aldrich

对氯苄胺

98%

别名:

1-(4-氟苯基)甲胺, 4-氯苯甲胺, 对氨基甲基基苯基氯, 对氯苄基胺, 对氯苯基甲胺, 对氯苯甲胺, (4-氯苯基)甲胺

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About This Item

线性分子式:
ClC6H4CH2NH2
CAS号:
分子量:
141.60
Beilstein:
507949
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

98%

形狀

liquid

折射率

n20/D 1.558 (lit.)

bp

215 °C (lit.)

密度

1.164 g/mL at 25 °C (lit.)

SMILES 字串

NCc1ccc(Cl)cc1

InChI

1S/C7H8ClN/c8-7-3-1-6(5-9)2-4-7/h1-4H,5,9H2

InChI 密鑰

YMVFJGSXZNNUDW-UHFFFAOYSA-N

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象形圖

CorrosionExclamation mark

訊號詞

Danger

危險聲明

危險分類

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

儲存類別代碼

8A - Combustible corrosive hazardous materials

水污染物質分類(WGK)

WGK 3

閃點(°F)

194.0 °F - closed cup

閃點(°C)

90 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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Two human metabolites of the REV-ERB agonist SR9009, identified by researchers with an interest in sports doping control, have been synthesized and assessed for purity. The synthesis employed was a modification of published procedures for the parent SR9009, careful attention
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S-benzylisothiourea 3a was discovered by its ability to inhibit indoleamine-2,3-dioxygenase (IDO) in our screening program. Subsequent optimization of the initial hit 3a lead to the identification of sub-muM inhibitors 3r and 10h, both of which suppressed kynurenine production in A431

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