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1015-18-5

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1015-18-5 Usage

Chemical Family

Alkylbenzenes

Physical State

Colorless liquid

Odor

Strong, pleasant

Common Uses

Fragrance and flavor industries; antibacterial and antifungal properties in household and personal care products

Additional Uses

Intermediate for the synthesis of various organic compounds

Safety Precautions

Can be harmful if ingested or inhaled; may cause skin and eye irritation

Check Digit Verification of cas no

The CAS Registry Mumber 1015-18-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,1 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1015-18:
(6*1)+(5*0)+(4*1)+(3*5)+(2*1)+(1*8)=35
35 % 10 = 5
So 1015-18-5 is a valid CAS Registry Number.

1015-18-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name rac-2,5-dimethyl-2-phenylhex-4-enal

1.2 Other means of identification

Product number -
Other names (+-)-2,5-Dimethyl-2-phenyl-hex-4-enal

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:1015-18-5 SDS

1015-18-5Relevant articles and documents

Diastereoselective synthesis of substituted hexahydrobenzo[de]isochromanes and evaluation of their antileishmanial activity

Saikia, Anil K.,Sultana, Sabera,Devi, Ngangbam Renubala,Deka, Manash J.,Tiwari, Kartikeya,Dubey, Vikash K.

supporting information, p. 970 - 979 (2016/01/15)

Hexahydrobenzo[de]isochromanes and hexahydropyrano[3,4,5-ij]isoquinolines can be efficiently synthesized via Friedel Crafts and oxa Pictet-Spengler reaction of acrylyl enol ethers mediated by triflic acid in good yields. The reaction is highly stereoselective. Two of the hexahydrobenzo[de]isochromanes are found to have moderate antileishmanial activity.

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