222402
甲基胍 盐酸盐
98%
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线性分子式:
CH3NHC(=NH)NH2·HCl
化学文摘社编号:
分子量:
109.56
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
98%
Form:
solid
InChI
1S/C2H7N3.ClH/c1-5-2(3)4;/h1H3,(H4,3,4,5);1H
SMILES string
Cl.CNC(N)=N
InChI key
VJQCNCOGZPSOQZ-UHFFFAOYSA-N
assay
98%
form
solid
solubility
water: soluble 50 mg/mL, clear
functional group
amine
Quality Level
Application
Methylguanidine hydrochloride can be used to prepare:
- Biaryl derivatives as BACE1 inhibitors.
- Modified xylose, which is used in the synthesis of biodegradable composite hydrogels.
- Methylguanidinium borohydride ionic liquid, which is applicable as a hydrogen storage material.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2
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
Jared N Cumming et al.
Bioorganic & medicinal chemistry letters, 22(7), 2444-2449 (2012-03-07)
From an initial lead 1, a structure-based design approach led to identification of a novel, high-affinity iminohydantoin BACE1 inhibitor that lowers CNS-derived Aβ following oral administration to rats. Herein we report SAR development in the S3 and F' subsites of
A non-covalent strategy for montmorillonite/xylose self-healing hydrogels
Qi X, et al.
Royal Society of Chemistry Advances, 5(51), 41006-41012 (2015)
Methylguanidinium borohydride: an ionic-liquid-based hydrogen-storage material
Doroodian A, et al.
Angewandte Chemie (International ed. in English), 49(10), 1871-1873 (2010)
Jovana Vušurović et al.
ChemistryOpen, 6(6), 739-750 (2017-12-12)
Interactions of ribonucleic acid (RNA) with guanidine and guanidine derivatives are important features in RNA-protein and RNA-drug binding. Here we have investigated noncovalently bound complexes of an 8-nucleotide RNA and six different ligands, all of which have a guanidinium moiety
Structure based design of iminohydantoin BACE1 inhibitors: identification of an orally available, centrally active BACE1 inhibitor
Cumming JN, et al.
Bioorganic & Medicinal Chemistry Letters, 22(7), 2444-2449 (2012)
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