Page last updated: 2024-12-06

alpha-naphthyl isocyanate

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

Alpha-naphthyl isocyanate is an organic compound with the formula C10H7NCO. It is a colorless liquid that is used as a reagent in organic synthesis. Alpha-naphthyl isocyanate is used in the synthesis of various compounds, such as polyurethanes and polymers. It is also used in the synthesis of pharmaceuticals and other chemicals. The compound is reactive and can undergo a variety of reactions. For example, it can react with alcohols to form carbamates and with amines to form ureas. alpha-naphthyl isocyanate is also used in the production of dyes, pigments, and resins. In the field of materials science, alpha-naphthyl isocyanate is employed in the synthesis of polymers with unique properties, such as high thermal stability and resistance to degradation. For example, it can be used in the preparation of polyurethanes, which are used in a wide range of applications, including foams, coatings, and adhesives. Alpha-naphthyl isocyanate is a versatile compound that is used in a variety of applications. Its reactivity and unique chemical properties make it a valuable tool in organic synthesis.'

alpha-naphthyl isocyanate: used to separate enantiomers of beta-blockers; structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID66589
CHEMBL ID2074791
SCHEMBL ID374
MeSH IDM0170831

Synonyms (54)

Synonym
.alpha.-naphthyl isocyanate
nsc4023
nsc-4023
1-isocyanatonaphthalene
86-84-0
1-naphthyl isocyanate ,
isocyanic acid, 1-naphthyl ester
naphthalene, 1-isocyanato-
alpha-naphthyl isocyanate
inchi=1/c11h7no/c13-8-12-11-7-3-5-9-4-1-2-6-10(9)11/h1-7
1-naphthyl isocyanate, 98%
STK399781
FT-0651962
isocyanic acid 1-naphthyl ester
I0125
AKOS000120750
1-isocyanato-naphthalene
einecs 201-703-7
unii-5lh2p0691e
5lh2p0691e ,
nsc 4023
ec 201-703-7
ai3-15382
30135-65-0
A820223
isocyanatonaphthalene
einecs 250-067-7
FT-0608118
AB00331
CHEMBL2074791
alpha-naphthylisocyanate
naphthyl isocyanate
1-naphthyl-isocyanate
l-naphthyl isocyanate
naphthylisocyanate
BBL027443
SCHEMBL374
1-naphthylisocyanate
1-naphthylisocyanate [mi]
naphthyl isocyanate, 1-
DTXSID9058949
W-104056
F2191-0305
mfcd00003881
1-naphthyl isocyanate, for hplc derivatization, >=99.0% (gc)
naphthalene, isocyanato-
naphthylisocyanat
(r)-alpha-cyanobenzylacetate
AS-14269
Q27262522
naphth-1-yl isocyanate
D91084
GEO-04573
EN300-20916

Research Excerpts

Dosage Studied

ExcerptRelevanceReference
" However, the increase in CCl(4) dosage significantly worsened survival."( Comparison of murine cirrhosis models induced by hepatotoxin administration and common bile duct ligation.
Chang, ML; Chang, PY; Chen, JC; Yeh, CT, 2005
)
0.33
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (5)

Assay IDTitleYearJournalArticle
AID681336TP_TRANSPORTER: cell accumulation of 0.05u daunomycin in MCF-7/ADR cells2004Journal of pharmaceutical sciences, Jul, Volume: 93, Issue:7
Effects of benzyl-, phenethyl-, and alpha-naphthyl isothiocyanates on P-glycoprotein- and MRP1-mediated transport.
AID680328TP_TRANSPORTER: Northern blot in vivo SD rat, liver2000American journal of physiology. Gastrointestinal and liver physiology, Mar, Volume: 278, Issue:3
Characterization of inducible nature of MRP3 in rat liver.
AID680324TP_TRANSPORTER: Northern blot in vivo SD rat, liver2000American journal of physiology. Gastrointestinal and liver physiology, Mar, Volume: 278, Issue:3
Characterization of inducible nature of MRP3 in rat liver.
AID679997TP_TRANSPORTER: Northern blot in vivo SD rat, liver2000American journal of physiology. Gastrointestinal and liver physiology, Mar, Volume: 278, Issue:3
Characterization of inducible nature of MRP3 in rat liver.
AID680323TP_TRANSPORTER: Western in vivo SD rat, liver2000American journal of physiology. Gastrointestinal and liver physiology, Mar, Volume: 278, Issue:3
Characterization of inducible nature of MRP3 in rat liver.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (18)

TimeframeStudies, This Drug (%)All Drugs %
pre-19902 (11.11)18.7374
1990's0 (0.00)18.2507
2000's9 (50.00)29.6817
2010's6 (33.33)24.3611
2020's1 (5.56)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 19.87

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index19.87 (24.57)
Research Supply Index3.00 (2.92)
Research Growth Index5.24 (4.65)
Search Engine Demand Index15.26 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (19.87)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (5.26%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other18 (94.74%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]