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92532-29-1

1,3-Benzenedimethanol, a-pentyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 92532-29-1 Structure

  • Basic information

    1. Product Name: 1,3-Benzenedimethanol, a-pentyl-
    2. Synonyms:
    3. CAS NO:92532-29-1
    4. Molecular Formula: C13H20O2
    5. Molecular Weight: 208.301
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 92532-29-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,3-Benzenedimethanol, a-pentyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,3-Benzenedimethanol, a-pentyl-(92532-29-1)
    11. EPA Substance Registry System: 1,3-Benzenedimethanol, a-pentyl-(92532-29-1)

  • 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: 92532-29-1(Hazardous Substances Data)

92532-29-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92532-29-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,5,3 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 92532-29:
(7*9)+(6*2)+(5*5)+(4*3)+(3*2)+(2*2)+(1*9)=131
131 % 10 = 1
So 92532-29-1 is a valid CAS Registry Number.

92532-29-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[3-(hydroxymethyl)phenyl]hexan-1-ol

1.2 Other means of identification

Product number -
Other names 3-(1-hydroxyhexyl)benzyl alcohol

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:92532-29-1 SDS

92532-29-1Downstream Products

92532-29-1Relevant articles and documents

Alkynes as activators in the nickel-catalysed addition of organoboronates to aldehydes

Takahashi, Go,Shirakawa, Eiji,Tsuchimoto, Teruhisa,Kawakami, Yusuke

, p. 1459 - 1461 (2007/10/03)

Alkynes act not as substrates but as co-catalysts in the presence of a nickel catalyst, an organoboronate and an aldehyde to promote the addition reaction between the substrates in combination with H2O. The Royal Society of Chemistry 2005.

Certain [3-(1-hydroxy hexyl-tetrahydro)naphthalenes], the corresponding naphthalenes having anti-inflammatory and anti-allergic activity

-

, (2008/06/13)

The invention relates to several aryloxy-alkane alcohols, for example 1-(3-(1-hydroxy-1-methylhexyl) phenoxy methyl)-2-methoxy-naphthalene, 2-(1-(3-(1-hydroxy-2,2-dimethylhexyl)phenoxy)ethyl naphthalene, 1-(3-6-phenoxy-1-hydroxyhexyl)phenoxy methyl)-4-methoxy naphthalene, 2-(3-(1-hydroxyhexyl) phenoxymethyl) naphthalene and 2-(3-(1-hydroxyhexyl)phenoxymethyl)-1,2,3,4-tetrahydro naphthalene, methods for their preparation and their use for treating inflammatory and allergic conditions in a mammal.

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