Spinacine, 98%

Name: Spinacine, 98% | 59981-63-4
Brand: J&K Chemical
SKU: JK305772_1_G
Price: 147.9 USD
Availability: InStock

Cat. No JK305772_1_G

Vendor: J&K Chemical

Product Information

Product Name

Spinacine, 98%

Brand Name

J&K

Product Number

305772

CAS

59981-63-4

Molecular Formula

C7H9N3O2

Molecular Weight

167.17

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

162899

IUPAC Name

(6S)-4,5,6,7-tetrahydro-3H-imidazo4,5-cpyridine-6-carboxylic acid

InChI Key

YCFJXOFFQLPCHD-YFKPBYRVSA-N

SMILES

C1C@H(NCC2=C1N=CN2)C(=O)O

Safety Information

Storage Condition

Store at 2-8℃

References Data Source From Pubchem

The LOTUS Initiative for Open Natural Products Research: frozen dataset union wikidata (with metadata)

Publication Date: 2026

DOI: 10.5281/zenodo.5794106

How formaldehyde reacts with amino acids

Publication Name: Communications Chemistry

Publication Date: 2019-11-07

DOI: 10.1038/s42004-019-0224-2

Flavonol and imidazole derivatives block HPV16 E6 activities and reactivate apoptotic pathways in HPV+ cells

Publication Name: Cell Death & Disease

Publication Date: 2016-01-21

DOI: 10.1038/cddis.2015.391

Direct chiral resolution of underivatized amino acids on a stationary phase dynamically modified with the ion‐exchanger Nτ‐decyl‐l‐spinacine

Publication Name: Journal of Separation Science

Publication Date: 2015-02-05

DOI: 10.1002/jssc.201401381

Synthesis and aggregation properties of a novel enzymatically resistant nucleoamino acid

Publication Name: Amino Acids

Publication Date: 2012-01-18

DOI: 10.1007/s00726-012-1219-9

Spinacine, 98%

Product Information

General Information

Safety Information

References Data Source From Pubchem

The LOTUS Initiative for Open Natural Products Research: frozen dataset union wikidata (with metadata)

How formaldehyde reacts with amino acids

Flavonol and imidazole derivatives block HPV16 E6 activities and reactivate apoptotic pathways in HPV+ cells

Direct chiral resolution of underivatized amino acids on a stationary phase dynamically modified with the ion‐exchanger Nτ‐decyl‐l‐spinacine

Synthesis and aggregation properties of a novel enzymatically resistant nucleoamino acid

Spinacine, 98%

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3-methoxy-L-phenylalanine

2-Ethynyl-1,3,5-trimethylbenzene, 97%

Tris-acetic acid electrophoresis buffer (50×TAE)

[S(R)]-N-[(1S)-1-[2-(Diadamantanphosphino)phenyl]ethyl]-N,2-dimethyl-2-propanesulfinamide, 95%

Mycophenolate Mofetil EP Impurity H

3-(4-Bromo-2-fluoro-3-methoxyphenyl)-3-oxo-propionic acid ethyl ester

Isochroman-1-carboxylic acid

Mycophenolate Mofetil

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Spinacine, 98%

Product Information

General Information

Safety Information

References Data Source From Pubchem

The LOTUS Initiative for Open Natural Products Research: frozen dataset union wikidata (with metadata)

How formaldehyde reacts with amino acids

Flavonol and imidazole derivatives block HPV16 E6 activities and reactivate apoptotic pathways in HPV+ cells

Direct chiral resolution of underivatized amino acids on a stationary phase dynamically modified with the ion‐exchanger Nτ‐decyl‐l‐spinacine

Synthesis and aggregation properties of a novel enzymatically resistant nucleoamino acid

Spinacine, 98%

Related Product

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3-methoxy-L-phenylalanine

2-Ethynyl-1,3,5-trimethylbenzene, 97%

Tris-acetic acid electrophoresis buffer (50×TAE)

[S(R)]-N-[(1S)-1-[2-(Diadamantanphosphino)phenyl]ethyl]-N,2-dimethyl-2-propanesulfinamide, 95%

Mycophenolate Mofetil EP Impurity H

3-(4-Bromo-2-fluoro-3-methoxyphenyl)-3-oxo-propionic acid ethyl ester

Isochroman-1-carboxylic acid

Mycophenolate Mofetil

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