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529249

Sigma-Aldrich

2-氯-1,3-二甲基氯化咪唑啉

for peptide synthesis

别名:

2-氯-4,5-二氢-1,3-二甲基-1 H -氯化咪唑, DMC

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About This Item

经验公式（希尔记法）:
C5H10Cl2N2
CAS号:
37091-73-9
分子量:
169.05
MDL號碼:
MFCD09039290
分類程式碼代碼:
12352005
PubChem物質ID:
24877665
NACRES:
NA.22

product name

2-氯-1,3-二甲基氯化咪唑啉,

形狀

crystalline

品質等級

100

反應適用性

reaction type: Coupling Reactions

mp

133-140 °C (lit.)

應用

peptide synthesis

官能基

chloro

SMILES 字串

[Cl-].CN1CC[N+](C)=C1Cl

InChI

1S/C5H10ClN2.ClH/c1-7-3-4-8(2)5(7)6;/h3-4H2,1-2H3;1H/q+1;/p-1

InChI 密鑰

AEBBXVHGVADBHA-UHFFFAOYSA-M

相关类别

應用

合成试剂：
标记葡萄糖作为支链寡糖合成的中间体
荧光化学传感器
1,2-二胺作为共激活剂相关精氨酸甲基转移酶 1 的抑制剂
变构葡萄糖激酶激活剂

用于合成以下物质的反应物：
伯胺中的有机叠氮化物

aza-Henry 反应试剂
用于 macroviracin A、cycloviracin B1 和环硅烷全合成的活化剂。

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險聲明

H315,H319,H335

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

从最新的版本中选择一种：

分析证书(COA)

Lot/Batch Number
MKCQ1285
MKCL7428
MKCK3746
MKBP8012V
MKBP1277V

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Journal of Organometallic Chemistry, 686, 175-182 (2003)
Ken Qin et al.
Bioorganic chemistry, 94, 103391-103391 (2019-11-26)
Thermostability of monoclonal antibodies (mAbs) and antibody-drug conjugates (ADCs), as a critical property of biotherapeutics, is important for their physicochemical processes, pharmacodynamics, and pharmacokinetics. Fc glycosylation of mAbs plays a crucial role in antibody functions including thermostability, however, due to
Alois Fürstner et al.
Journal of the American Chemical Society, 125(43), 13132-13142 (2003-10-23)
The first total synthesis of the antivirally active glycolipid cycloviracin B(1) (1) is described. The approach is based on a two-directional synthesis strategy which constructs the C(2)()-symmetrical macrodiolide core of the target by an efficient template-directed macrodilactonization reaction promoted by
Yanzi Gou et al.
Journal of polymer science. Part A, Polymer chemistry, 51(12), 2588-2597 (2013-06-14)
Synthetic glycopolymers are important natural oligosaccharides mimics for many biological applications. To develop glycopolymeric drugs and therapeutic agents, factors that control the receptor-ligand interaction need to be investigated. A library of well-defined glycopolymers has been prepared by the combination of
Shunya Takahashi et al.
The Journal of organic chemistry, 69(13), 4509-4515 (2004-06-19)
The C(2)-symmetric macrodiolide core 2 of an antiviral agent, macroviracin A (1), was constructed in a single step by the intermolecular macrodimerization of C(22)-hydroxy carboxylic acid 3 with 2-chloro-1,3-dimethylimidazolinium chloride and DMAP in the presence of sodium hydride (NaH). The
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Imidazolium Derived Reagents

N-Acylimidazoles were recognized in the early 1950s as reactive intermediates suitable for the acylation of amino compounds. The search for better coupling reagents than DCC led to the development of CDI (1,1’-carbonyldiimidazole) and related carbonylimidazoles.

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