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O-Geranylvanillin is a vanillin derivative that serves as a flavoring agent and fragrance ingredient. It is characterized by its sweet, vanilla-like aroma and is synthesized from geranyl acetone and vanillin through a condensation reaction. Known for its strong and long-lasting scent, O-Geranylvanillin is a versatile chemical compound used in various consumer products.

151455-08-2

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151455-08-2 Usage

Uses

Used in the Fragrance Industry:
O-Geranylvanillin is used as a fragrance ingredient for its sweet, vanilla-like aroma, contributing to the scent profiles of perfumes, soaps, and other scented products. Its strong and long-lasting scent makes it a popular choice in this industry.
Used in the Food Industry:
O-Geranylvanillin is used as a flavoring agent in the food industry, particularly in the production of confectionery, baked goods, and beverages. Its pleasant aroma and flavor enhance the taste and smell of these products, making it a widely used compound in food manufacturing.

Check Digit Verification of cas no

The CAS Registry Mumber 151455-08-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,4,5 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 151455-08:
(8*1)+(7*5)+(6*1)+(5*4)+(4*5)+(3*5)+(2*0)+(1*8)=112
112 % 10 = 2
So 151455-08-2 is a valid CAS Registry Number.
InChI:InChI=1/C18H24O3/c1-14(2)6-5-7-15(3)10-11-21-17-9-8-16(13-19)12-18(17)20-4/h6,8-10,12-13H,5,7,11H2,1-4H3/b15-10+

151455-08-2SDS

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 Geranyloxyvanillin

1.2 Other means of identification

Product number -
Other names 4-((3,7-Dimethylocta-2,6-dien-1-yl)oxy)-3-methoxybenzaldehyde

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:151455-08-2 SDS

151455-08-2Downstream Products

151455-08-2Relevant academic research and scientific papers

Synthesis of O-prenylated and O-geranylated derivatives of 5-benzylidene2,4-thiazolidinediones and evaluation of their free radical scavenging activity as well as effect on some phase II antioxidant/detoxifying enzymes

Hossain, Sk. Ugir,Bhattacharya, Sudin

, p. 1149 - 1154 (2007)

A series of 5-arylidene-2,4-thiazolidinediones and its geranyloxy or prenyloxy derivative were synthesized and studied for their radical scavenging activity using 1,1-diphenyl-2-picrylhydrazyl (DPPH) assay. Their comparable scavenging activities were expr

NOVEL SUGAR-DERIVED GELATOR

-

Paragraph 0133; 0134; 0141, (2015/02/18)

There is provided a novel gelator containing a sugar derivative. A gelator including a compound of Formula (1) or Formula (2): wherein each of R1 and R3 is independently a linear or branched alkyl group having a carbon atom number of 1 to 20, a cyclic C3-20 alkyl group, or a linear or branched alkenyl group having a carbon atom number of 2 to 20, n is 0 or an integer of 1 to 4, R2 is a hydrogen atom, a linear or branched alkyl group having a carbon atom number of 1 to 10, or an aryl group optionally having a substituent, and R4 and R5 are each a hydroxy group.

Nelumal A, the active principle from Ligularia nelumbifolia, is a novel farnesoid X receptor agonist

Epifano, Francesco,Genovese, Salvatore,James Squires,Gray, Matthew A.

scheme or table, p. 3130 - 3135 (2012/06/04)

A series of 29 oxyprenylated and azoprenylated phenylpropanoids were chemically synthesized and tested in transfected cultured HepG2 cells by means of the dual-luciferase assay as farnesoid X receptor (FXR) agonists, using the endogenous ligand chenodeoxy

Convenient synthesis of (E)-methyl O-alkylferulates: Formal synthesis of O-geranylconiferyl alcohol, a metabolite of Fagara rhetza

Mahajan, Rajesh P.,Patil, Shamkant L.,Mali, Raghao S.

, p. 328 - 331 (2007/10/03)

A convenient two step stereoselective synthesis of (E)-methyl O-alkylferulate 5a-c is described from vanillin 1. Reaction of vanillin 1 with allyl-, prenyl- or geranyl- bromide 2a-c has afforded alkyl ethers 3a-c which on reaction with phosphorane 4, under microwave irradiation, gives (E)-methyl O-alkylferulates 5a-c in high yield. In an alternative approach vanillin 1 on reaction with phosphorane 4 provides (E)-methyl ferulate 6 which on reaction with the corresponding bromides 2a-c gives (E)-methyl O-alkylferulates 5a-c.

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