496871
1,3-二(叔丁氧基羰基)胍
98%
别名:
C,C′-Bis(1,1-dimethylethyl) N,N′-(carbonimidoyl)bis[carbamate], Di-Boc-guanidine, N,N′-Bis(Boc)guanidine, N,N′-Di-Boc-guanidine, N1,N2-Bis(tert-butoxycarbonyl)guanidine, N1,N2-Bis(tert-butyloxycarbonyl)guanidine, tert-Butyl [N-(tert-butoxycarbonyl)carbamimidoyl]carbamate
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关于此项目
线性分子式:
HN=C[NHCO2C(CH3)3]2
化学文摘社编号:
分子量:
259.30
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
产品名称
1,3-二(叔丁氧基羰基)胍, 98%
InChI
1S/C11H21N3O4/c1-10(2,3)17-8(15)13-7(12)14-9(16)18-11(4,5)6/h1-6H3,(H3,12,13,14,15,16)
SMILES string
CC(C)(C)OC(=O)NC(=N)NC(=O)OC(C)(C)C
InChI key
VPWFNCFRPQFWGS-UHFFFAOYSA-N
assay
98%
mp
141-144 °C (lit.)
functional group
amine
Quality Level
Application
1,3-Bis(tert-butoxycarbonyl)guanidine may be used to produce a guanidinyl derivative during the multi-step synthesis of (-)-crispine E. It may also be used as a reagent during the preparation of 1,6-diphenylnaphthalenes.
General description
1,3-Bis(tert-butoxycarbonyl)guanidine is a guanidine derivative. The synthesis of N-substituted 2-aminoimidazole inhibitors using 1,3-bis(tert-butoxycarbonyl)guanidine has been reported.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Yongzheng Zhang et al.
Bioorganic & medicinal chemistry letters, 23(7), 2001-2006 (2013-03-14)
Bacterial cell division occurs in conjunction with the formation of a cytokinetic Z-ring structure comprised of FtsZ subunits. Agents that disrupt Z-ring formation have the potential, through this unique mechanism, to be effective against several of the newly emerging multidrug-resistant
Andrew A Yeagley et al.
Organic & biomolecular chemistry, 11(1), 130-137 (2012-10-19)
Antibiotic resistance is a significant problem and is compounded by the ability of many pathogenic bacteria to form biofilms. A library of N-substituted derivatives of a previously reported 2-aminoimidazole/triazole (2-AIT) biofilm modulator was constructed via α-bromoketone cyclization with 1,3-bis(tert-butoxycarbonyl)guanidine, followed
Synthesis of (-)-Trolline,(-)-Crispin A and (-)-Crispine E.
Kanemitsu T, et al.
Heterocycles, 74, 199-204 (2008)
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