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84099-58-1

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84099-58-1 Usage

General Description

4,5,6,7-tetrahydrobenzofuran-4-ol is a chemical compound belonging to the class of organic compounds known as benzofurans. Benzofurans are compounds containing a benzene ring fused to a furan. This particular compound has a tetrahydro structure, which means it includes a specific structure of four Hydrogen atoms. While further details on its functionality and use may vary, its presence in such a fused structure may make it relevant in different applications in the chemical industry or in research. However, detailed specifics about its uses, safety, or potential benefits are not easily available and may require further research or consultation of specialized industry information.

Check Digit Verification of cas no

The CAS Registry Mumber 84099-58-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,0,9 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 84099-58:
(7*8)+(6*4)+(5*0)+(4*9)+(3*9)+(2*5)+(1*8)=161
161 % 10 = 1
So 84099-58-1 is a valid CAS Registry Number.

84099-58-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5,6,7-tetrahydro-1-benzofuran-4-ol

1.2 Other means of identification

Product number -
Other names 4,5,6,7-tetrahydrobenzofuran-4-ol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:84099-58-1 SDS

84099-58-1Relevant articles and documents

BICYCLIC HETEROARYL SUBSTITUTED COMPOUNDS

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Page/Page column 334; 335, (2018/03/25)

Disclosed are compounds of Formula (I) to (VIII): (I) (II) (III) (IV) (V) (VI) (VII) (VIII); or a stereoisomer, tautomer, pharmaceutically acceptable salt, solvate or prodrug thereof, wherein R3 is a bicyclic heteroaryl group substituted with zero to 3 R3a; and R1, R2, R3a, R4, and n are defined herein. Also disclosed are methods of using such compounds as PAR4 inhibitors, and pharmaceutical compositions comprising such compounds. These compounds are useful in inhibiting or preventing platelet aggregation, and are useful for the treatment of a thromboembolic disorder or the primary prophylaxis of a thromboembolic disorder.

SELECTIVE REDUCTION OF ALDEHYDES AND KETONES

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Page/Page column 47; 48; 49, (2017/12/01)

The present invention relates to a selective reduction of specific aldehydes and ketones to their corresponding alcohols.

Selective hydrogenation of unsaturated carbonyls by Ni-Fe-based alloy catalysts

Putro, Wahyu S.,Kojima, Takashi,Hara, Takayoshi,Ichikuni, Nobuyuki,Shimazu, Shogo

, p. 3637 - 3646 (2017/08/21)

Ni-Fe alloy catalysts prepared by a simple hydrothermal method and subsequent H2 treatment exhibited the greatest activity and selectivity for the hydrogenation of biomass-derived furfural to furfuryl alcohol among the examined second metals, such as Al, Ga, In, Co, and Ti. This work reveals that the alloying of Ni and Fe is a key factor in achieving highly selective hydrogenation of the CO moiety in unsaturated carbonyl substrates. We found that decreasing the temperature of H2 treatment (i.e. decreasing the crystallite size), e.g. Ni-Fe(2)HT-573 K (TOF = 952 h-1), increased the activity compared to that over Ni-Fe(2)HT-673 (TOF = 375 h-1) for furfural hydrogenation. This result suggests that a low-coordinated Ni-Fe alloy was imperative for the catalytic cycle. Moreover, the effect of the metal/support interface was critical; despite the high catalytic performance of Ni-Fe/TiO2, Ni-Fe/Al2O3, and Ni-Fe/CeO2, Ni-Fe supported on SiO2, taeniolite, and hydrotalcite catalysts were ineffective. Vibrational studies using FT-IR measurement confirmed that furfural was physically adsorbed on the surface of the Ni-Fe alloy catalyst via an η1(O) configuration. The synthetic scope of the Ni-Fe catalytic system was very broad; various types of unsaturated carbonyls, such as unsaturated aromatics, unconjugated aliphatics, and a large substituent, were selectively converted into the corresponding unsaturated alcohols.

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