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33467-79-7

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33467-79-7 Usage

Uses

2,4-Heptadien-1-ol can be used in nut or spice blends. It is used as a flavoring ingredient.

Aroma threshold values

Medium strength odor, fatty type; recommend smelling in a 1.00% solution or less.

Check Digit Verification of cas no

The CAS Registry Mumber 33467-79-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,4,6 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 33467-79:
(7*3)+(6*3)+(5*4)+(4*6)+(3*7)+(2*7)+(1*9)=127
127 % 10 = 7
So 33467-79-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H12O/c1-2-3-4-5-6-7-8/h3-6,8H,2,7H2,1H3/b4-3+,6-5+

33467-79-7 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Alfa Aesar

  • (15765)  2,4-Heptadien-1-ol   

  • 33467-79-7

  • 5g

  • 646.0CNY

  • Detail
  • Alfa Aesar

  • (15765)  2,4-Heptadien-1-ol   

  • 33467-79-7

  • 25g

  • 2384.0CNY

  • Detail

33467-79-7SDS

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 2,4-HEPTADIEN-1-OL

1.2 Other means of identification

Product number -
Other names hepta-2t,4t-dien-1-ol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:33467-79-7 SDS

33467-79-7Relevant articles and documents

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Bestmann,H.J. et al.

, p. 2467 - 2470 (1979)

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Asymmetric synthesis of 3,3,5,5-tetrasubstituted 1,2-dioxolanes: Total synthesis of epiplakinic acid F

Tian, Xiang-Yin,Han, Jian-Wei,Zhao, Qiong,Wong, Henry N. C.

, p. 3686 - 3700 (2014/06/09)

The first enantioselective total synthesis of epiplakinic acid F (1) was achieved through a pivotal step involving a radical-mediated asymmetric peroxidation of vinylcyclopropanes with molecular oxygen to construct highly substituted 1,2-dioxolanes. Subsequent conversions of the chiral 1,2-dioxolanes led to total synthesis of epiplakinic acid F (1) and the confirmation of its absolute configuration. The enantiomer of epiplakinic acid F methyl ester (2) was also prepared. This journal is the Partner Organisations 2014.

Synthesis of plastoquinone derivatives with different structures of the side chain

Liu, Benli,Gu, Lianquan,Zhang, Jingling

, p. 104 - 110 (2007/10/02)

Two schemes for the synthesis of plastoquinone derivatives with ω-substituted alkyl side chains have been developed, based on radical alkylation of 2,3-dimethyl-1,4-benzoquinone with ω-substituted carboxylic and/or dicarboxylic acids in the presence of S2O82- and Ag+.In Scheme 1, radical alkylation of 2,3-dimethyl-1,4-benzoquinone with 11-bromoundecanoic acid, in the presence of (NH4)2S2O8 and AgNO3, gave 2,3-dimethyl-5-(10-bromodecyl)-1,4-benzoquinone, which, after hydration, gave 2,3-dimethyl-5-(10-hydroxydecyl)-1,4-benzoquinone.Esterification of 2,3-dimethyl-5-(10-hydroxydecyl)-1,4-benzoquinone with different acyl chlorides gave 2,3-dimethyl-5-(10-acyloxydecyl)-1,4-benzoquinone.In Scheme 2, radical alkylation of 2,3-dimethyl-1,4-benzoquinone with adipic acid, in the presence of K2S2O8 and AgNO3, gave 2,3-dimethyl-5-(4-carboxybutyl)-1,4-benzoquinone, which was converted to 2,3-dimethyl-5--1,4-benzoquinone by esterification with different alcohols in the presence of dicyclohexylcarbodiimide. 2,3-Dimethyl-5-(8-carboxyoctyl)-1,4-benzoquinone and 2,3-dimethyl-5--1,4-benzoquinone were similarly synthesized from 2,3-dimethyl-1,4-benzoquinone and sebacic acid.Plastoquinone derivatives having different kinds of double bonds in the side chain with and without a 6-methyl group were synthesized from 2,3,5-trimethyl-1,4-benzoquinone and 2,3-dimethyl-1,4-benzoquinone by successive reactions with (1) NaBH4; (2) KHSO4, different kinds of allylic alcohols; (3) Ag2O.The allylic alcohols were prepared from their corresponding aldehydes by reduction with NaBH4. 2,3,6-Trimethyl-1,4-benzoquinone by radical methylation with acetic acids in the presence of K2S2O8 + AgNO3.

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