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501086-15-3

Pilosol A is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 501086-15-3 Structure

  • Basic information

    1. Product Name: Pilosol A
    2. Synonyms: Pilosol A;(R)-(-)-7-Phenylhepta-4,6-diyn-2-ol
    3. CAS NO:501086-15-3
    4. Molecular Formula: C13H12O
    5. Molecular Weight: 184.23378
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 501086-15-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 332.0±34.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.08±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 14.18±0.20(Predicted)
    10. CAS DataBase Reference: Pilosol A(CAS DataBase Reference)
    11. NIST Chemistry Reference: Pilosol A(501086-15-3)
    12. EPA Substance Registry System: Pilosol A(501086-15-3)

  • 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: 501086-15-3(Hazardous Substances Data)

501086-15-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 501086-15-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,0,8 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 501086-15:
(8*5)+(7*0)+(6*1)+(5*0)+(4*8)+(3*6)+(2*1)+(1*5)=103
103 % 10 = 3
So 501086-15-3 is a valid CAS Registry Number.

501086-15-3SDS

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 (R)-7-phenylhepta-4,6-diyn-2-ol

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:501086-15-3 SDS

501086-15-3Downstream Products

501086-15-3Relevant articles and documents

One-pot synthesis and functionalization of polyynes via alkylidene carbenoids

Luu, Thanh,Morisaki, Yasuhiro,Tykwinski, Rik R.

, p. 1158 - 1162 (2008/12/22)

A one-pot, two-step method for the synthesis of diynes and triynes is reported. The reaction of a dibromoolefinic precursor with BuLi effects a Fritsch-Buttenberg-Wiechell rearrangement and generates a lithium acetylide intermediate, which is then trapped

One-pot formation and derivatization of di- and triynes based on the Fritsch-Buttenberg-Wiechell rearrangement

Luu, Thanh,Morisaki, Yasuhiro,Cunningham, Nina,Tykwinski, Rik R.

, p. 9622 - 9629 (2008/03/15)

(Chemical Equation Presented) A divergent, one-pot synthesis of functionalized polyynes has been developed. Beginning with the appropriately substituted dibromoolefinic precursor, a carbenoid Fritsch-Buttenberg-Wiechell (FBW) rearrangement is used to gene

A one-pot synthesis and functionalization of polyynes

Morisaki, Yasuhiro,Luu, Thanh,Tykwinski, Rik R.

, p. 689 - 692 (2007/10/03)

A one-pot synthesis and derivatization of diynes and triynes is reported. The polyyne framework is formed from a dibromoolefin precursor based on a carbenoid rearrangement, and the resulting Li-acetylide is then trapped in situ with an electrophile to pro

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