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1H-inden-1-ylmethanol, with the chemical formula C10H10O, is a colorless liquid characterized by a pleasant odor. It is a versatile chemical compound that plays a significant role in the synthesis of various organic compounds. Additionally, it is recognized for its potential biological activities, such as antibacterial and antifungal properties. Due to its potential hazards if not handled properly, care should be taken during its use.

2471-88-7

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2471-88-7 Usage

Uses

Used in Organic Synthesis:
1H-inden-1-ylmethanol is used as a key intermediate in the synthesis of various organic compounds, contributing to the development of new chemical entities for different applications.
Used in Fragrance Industry:
1H-inden-1-ylmethanol is used as a fragrance ingredient in perfumes and other personal care products, adding to their pleasant scent profiles.
Used in Pharmaceutical Research:
1H-inden-1-ylmethanol is studied for its potential biological activities, such as its antibacterial and antifungal properties, indicating its possible use in the development of new antimicrobial agents.

Check Digit Verification of cas no

The CAS Registry Mumber 2471-88-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,7 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2471-88:
(6*2)+(5*4)+(4*7)+(3*1)+(2*8)+(1*8)=87
87 % 10 = 7
So 2471-88-7 is a valid CAS Registry Number.

2471-88-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-inden-1-ylmethanol

1.2 Other means of identification

Product number -
Other names Indene-1-methanol

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:2471-88-7 SDS

2471-88-7Relevant academic research and scientific papers

High Anionic Polymerizability of Benzofulvene: New Exo-Methylene Hydrocarbon Monomer

Kosaka, Yuki,Kawauchi, Susumu,Goseki, Raita,Ishizone, Takashi

, p. 4421 - 4430 (2015/07/28)

The anionic polymerization of benzofulvene (BF) quantitatively proceeded with various initiators, such as sec-BuLi, diphenylmethyllithium, diphenylmethylpotassium, triphenylmethyllithium, and triphenylmethylpotassium, in THF at -78 °C to give polymers having predicted molecular weights based on the molar ratios between BF and the initiators and narrow molecular weight distributions (MWD, Mw/Mn 1H and 13C NMR analyses revealed that the repeating units of poly(BF) consisted of a 1,2-addition unit and a 1,4-addition unit without a 3,4-addition unit regardless of the polymerization conditions. The exo-methylene moiety (CH2=) of BF always participated in the addition polymerization. The addition modes were dependent on the polymerization temperature and not on the solvent or the countercation of the anionic initiator. For instance, polymer obtained with sec-BuLi in THF at 40°C contained 72% of the 1,4-addition unit and 28% of the 1,2-addition unit. Therefore, BF acted as a polymerizable 1,3-diene possessing a fixed transoid framework.

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