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1013027-15-0

1-(3-(hydroxymethyl)phenyl)ethan-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1013027-15-0 Structure

  • Basic information

    1. Product Name: 1-(3-(hydroxymethyl)phenyl)ethan-1-ol
    2. Synonyms: 1-(3-(hydroxymethyl)phenyl)ethan-1-ol
    3. CAS NO:1013027-15-0
    4. Molecular Formula:
    5. Molecular Weight: 152.193
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1013027-15-0.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-(hydroxymethyl)phenyl)ethan-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(3-(hydroxymethyl)phenyl)ethan-1-ol(1013027-15-0)
    11. EPA Substance Registry System: 1-(3-(hydroxymethyl)phenyl)ethan-1-ol(1013027-15-0)

  • 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: 1013027-15-0(Hazardous Substances Data)

1013027-15-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1013027-15-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,3,0,2 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1013027-15:
(9*1)+(8*0)+(7*1)+(6*3)+(5*0)+(4*2)+(3*7)+(2*1)+(1*5)=70
70 % 10 = 0
So 1013027-15-0 is a valid CAS Registry Number.

1013027-15-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1'-hydroxyethyl)-benzyl alcohol

1.2 Other means of identification

Product number -
Other names -

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:1013027-15-0 SDS

1013027-15-0Relevant articles and documents

Synthesis and evaluation of multi-functional NO-donor/insulin-secretagogue derivatives for the treatment of type II diabetes and its cardiovascular complications

Digiacomo, Maria,Martelli, Alma,Testai, Lara,Lapucci, Annalina,Breschi, Maria C.,Calderone, Vincenzo,Rapposelli, Simona

, p. 422 - 428 (2015)

Although there is a significant effort in the discovery of effective therapies to contrast both the pathological endocrine and metabolic aspects of diabetes and the endothelial dysfunction associated with this disease, no hypoglycemic drug has been proven

Iron Catalyzed Hydroboration of Aldehydes and Ketones

Tamang, Sem Raj,Findlater, Michael

, p. 12857 - 12862 (2017/12/08)

We report an operationally convenient room temperature hydroboration of aldehydes and ketones employing Fe(acac)3 as precatalyst. The hydroboration of aldehydes and ketones proceeded efficiently at room temperature to yield, after work up, 1° and 2° alcohols; chemoselective hydroboration of aldehydes over ketones is attained under these conditions. We propose a σ-bond metathesis mechanism in which an Fe-H intermediate is postulated to be a key reactive species.

Evaluation of the NO-releasing properties of NO-donor linkers

Calderone, Vincenzo,Digiacomo, Maria,Martelli, Alma,Minutolo, Filippo,Rapposelli, Simona,Testai, Lara,Balsamo, Aldo

, p. 189 - 195 (2008/09/20)

This work describes the synthesis of some benzoic (1-4) and alcoholic (5-7) nitrooxy derivatives, which are nitric oxide (NO) donors in themselves, and can also be seen as useful linkers that can be used in multi-target drugs capable of releasing NO. The

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