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2,6,6-TRIMETHYL-HEPT-4-YN-3-OL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90975-00-1

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90975-00-1 Usage

Physical state

Colorless liquid

Odor

Strong

Primary uses

Flavor and fragrance ingredient in food and cosmetic industries

Secondary uses

Intermediate in the synthesis of other chemical compounds

Hazards

Flammable, harmful if inhaled or swallowed, can cause skin and eye irritation

Safety precautions

Handle and store with proper safety measures to prevent accidents or exposure.

Check Digit Verification of cas no

The CAS Registry Mumber 90975-00-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,9,7 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 90975-00:
(7*9)+(6*0)+(5*9)+(4*7)+(3*5)+(2*0)+(1*0)=151
151 % 10 = 1
So 90975-00-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O/c1-8(2)9(11)6-7-10(3,4)5/h8-9,11H,1-5H3

90975-00-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6,6-trimethylhept-4-yn-3-ol

1.2 Other means of identification

Product number -
Other names 2,6,6-trimethyl-hept-4-yn-3-ol

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:90975-00-1 SDS

90975-00-1Relevant academic research and scientific papers

Chromium(II) Reagents; 1. Reduction of α-Acetylenic Ketones to trans-Enones

Smith, Amos B.,Levenberg, Patricia A.,Suits, Joan Z.

, p. 184 - 189 (2007/10/02)

The preparation and chromium(II)-induced reduction of twelve α-acetylenic ketones are reported.In general only trans-olefinic products were observed; the yields ranged from 40-84percent.A particular advantage of this protocol is its selectivity, thereby permitting use with a wide variety of functionalities.

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