187264-03-5

• 

• Basic information

  1. Product Name: 1-PHENYLMETHYL-1H-INDOLE-2-METHANOL
  2. Synonyms: 1-PHENYLMETHYL-1H-INDOLE-2-METHANOL;1(-PHENYLMETHYL)-1H-INDOLE-2-MATHANOL;(1-Benzylindol-2-yl)methanol
  3. CAS NO:187264-03-5
  4. Molecular Formula: C₁₆H₁₅NO
  5. Molecular Weight: 237.3
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 187264-03-5.mol
  9. Article Data: 14

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 456°Cat760mmHg
  3. Flash Point: 229.6°C
  4. Appearance: /
  5. Density: 1.11g/cm³
  6. Vapor Pressure: 4.15E-09mmHg at 25°C
  7. Refractive Index: 1.606
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. PKA: 14.96±0.10(Predicted)
  11. CAS DataBase Reference: 1-PHENYLMETHYL-1H-INDOLE-2-METHANOL(CAS DataBase Reference)
  12. NIST Chemistry Reference: 1-PHENYLMETHYL-1H-INDOLE-2-METHANOL(187264-03-5)
  13. EPA Substance Registry System: 1-PHENYLMETHYL-1H-INDOLE-2-METHANOL(187264-03-5)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 187264-03-5(Hazardous Substances Data)

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• Downstream Products
• Article

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• 1(-BENZYL)-1H-INDOLE-2-MATHANOLCAS

  Cas No: 187264-03-5

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• 1(-PHENYLMETHYL)-1H-INDOLE-2-METHANOL

  Cas No: 187264-03-5

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187264-03-5 Usage

Classification

A chemical compound belonging to the indole class.

Molecular weight

297.4 g/mol.

Type

Synthetic substance.

Usage

Commonly used in research and chemical synthesis.

Applications

Development of pharmaceuticals and agrochemicals.

Pharmacological properties

Potential antioxidant and anti-inflammatory effects.

Precursor potential

Investigated for its potential use as a precursor in the synthesis of various biologically active compounds.

Versatility

Has potential applications in various fields of science and technology.

Check Digit Verification of cas no

The CAS Registry Mumber 187264-03-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,7,2,6 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 187264-03:
(8*1)+(7*8)+(6*7)+(5*2)+(4*6)+(3*4)+(2*0)+(1*3)=155
155 % 10 = 5
So 187264-03-5 is a valid CAS Registry Number.

InChI:InChI=1/C16H15NO/c18-12-15-10-14-8-4-5-9-16(14)17(15)11-13-6-2-1-3-7-13/h1-10,18H,11-12H2

187264-03-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name	(1-benzylindol-2-yl)methanol

1.2 Other means of identification

Product number	-
Other names	1-phenylmethyl-1h-indole-2-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:187264-03-5 SDS

187264-03-5Upstream product

• 100-39-0 benzyl bromide 
• 1477-50-5 Indole-2-carboxylic acid 
• 3770-50-1 2-carbethoxyindole 
• 81787-92-0 1-benzyl-1H-indole-2-carboxylic acid methyl ester 
• 17017-66-2 ethyl 1-benzyl-1H-indole-2-carboxylate 

187264-03-5Downstream Products

• 940960-51-0 2-(allyloxymethyl)-1-benzyl-1H-indole 
• 1073968-37-2 9-benzyl-4-methyl-9H-carbazole 
• 1305306-04-0 C₂₀H₁₇N 
• 17901-58-5 1-benzyl-2-methyl-1H-indole 
• 1431570-01-2 methyl 1-benzyl-2-(2-methoxy-2-oxoethyl)-1H-indole-3-carboxylate 

187264-03-5Relevant articles and documents

Design, synthesis and biological evaluation of novel indole-xanthendione hybrids as selective estrogen receptor modulators

Singla, Ramit,Gupta, Kunj Bihari,Upadhyay, Shishir,Dhiman, Monisha,Jaitak, Vikas

, p. 266 - 277 (2017/12/06)

Ground breaking clinical therapeutic advances in the treatment of breast cancer (BC) is the introduction of selective estrogen receptor modulators (SERMs). We have expeditiously designed and synthesized indole-xanthendione hybrids by coalescing the indole

Identification of novel indole based heterocycles as selective estrogen receptor modulator

Singla, Ramit,Prakash, Kunal,Bihari Gupta, Kunj,Upadhyay, Shishir,Dhiman, Monisha,Jaitak, Vikas

, p. 72 - 88 (2018/05/09)

In the present study, we have designed and synthesized indole derivatives by coalescing the indole nucleus with chromene carbonitrile and dihydropyridine nucleus. Two compounds 5c and 6d were selected from series I and II after sequential combinatorial li

Cycloaddition of in Situ Formed Azaoxyallyl Cations with 2-Alkenylindoles: An Approach to Tetrahydro-β-carbolinones

Zhang, Kaifan,Xu, Xiaoying,Zheng, Jiuan,Yao, Hequan,Huang, Yue,Lin, Aijun

supporting information, p. 2596 - 2599 (2017/05/24)

A novel [3 + 3] cycloaddition between in situ formed azaoxyallyl cations and 2-alkenylindoles has been developed. This concise method allows the efficient construction of a series of tetrahydro-β-carbolinones in good yields under mild conditions. Gram-sca

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