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30316-18-8

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30316-18-8 Usage

Physical state

Colorless, crystalline compound

Odor

Floral

Primary use

Fragrance ingredient in perfumes and personal care products

Additional use

Flavoring agent in food products

Application

Chemical intermediate in the production of other compounds

Toxicity

Low toxicity

Safety

Generally recognized as safe (GRAS) for use in consumer products when used in accordance with regulations and guidelines

Check Digit Verification of cas no

The CAS Registry Mumber 30316-18-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,3,1 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 30316-18:
(7*3)+(6*0)+(5*3)+(4*1)+(3*6)+(2*1)+(1*8)=68
68 % 10 = 8
So 30316-18-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H16/c1-9-4-7-12-10(2)5-6-11(3)13(12)8-9/h5-6,8H,4,7H2,1-3H3

30316-18-8SDS

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 3,5,8-trimethyl-1,2-dihydronaphthalene

1.2 Other means of identification

Product number -
Other names 1,2-dihydro-3,5,8-trimethyl-naphthalene

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:30316-18-8 SDS

30316-18-8Relevant articles and documents

A new synthesis of 4-(2,3,6-trimethylphenyl)butan-2-ol, a C13-norisoprenoid artifact from Vitis vinifera linn. and its conversion to several terpenic natural products of plant and marine origin

Sudalai, A.,Rao, Krishna G. S.

, p. 110 - 112 (2007/10/02)

The four-step synthesis of 4-(2,3,6-trimethylphenyl)butan-2-ol (1), starts from 5,8-dimethyl-3,4-dihydro-2-naphthaldehyde (2).The trimethyldihydronaphthalene (10) obtained from the reduction of 2 is ozonised to the keto aldehyde (11), which is reduced to

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