34169-70-5 Usage
Uses
Used in Fragrance Industry:
Iso E Super is used as a key ingredient in the production of perfumes and colognes for its woody, musky, and slightly floral scent. Its long-lasting aroma and ability to enhance and amplify other fragrance notes make it a valuable component in creating complex and captivating fragrances.
Used in Personal Care and Beauty Products:
Iso E Super is used as a fragrance ingredient in various personal care and beauty products, such as skincare, haircare, and makeup, due to its unique scent and ability to improve the longevity of other fragrances in these products.
Used in Household and Industrial Applications:
Iso E Super is also used in household and industrial applications, such as air fresheners, cleaning products, and textiles, for its long-lasting and pleasant scent, as well as its ability to enhance the fragrance of other ingredients in these products.
Check Digit Verification of cas no
The CAS Registry Mumber 34169-70-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,1,6 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 34169-70:
(7*3)+(6*4)+(5*1)+(4*6)+(3*9)+(2*7)+(1*0)=115
115 % 10 = 5
So 34169-70-5 is a valid CAS Registry Number.
InChI:InChI=1/C15H20O3/c1-8-7-11-12(9(2)10(8)5-6-16)14(18)15(3,4)13(11)17/h7,13,16-17H,5-6H2,1-4H3/t13-/m1/s1
34169-70-5Relevant academic research and scientific papers
Chemical and Chemotaxonomical Studies of Ferns. LIV. Pterosin Derivatives of the Genus Microlepia (Pteroidaceae)
Kuraishi, Tadayuki,Murakami, Takao,Taniguchi, Takao,Kobuki, Yohko,Maehashi, Haruka,et al.
, p. 2305 - 2312 (2007/10/02)
From the fronds of five pteridaceous ferns , several 1-indanone-type sesquiterpenes (pterosins and pterosides) were isolated.Four of them, isolated from M. speluncae were new and were assigned the structures 13-hydroxy-3(R)-pterosin D (V), 13-hydroxy-3(R)-pterosin D 3-O-α-L-arabinopyranoside (VI), 3(R)-pterosin D 3-O-α-L-arabinopyranoside (VIII) and 2(R),3(R)-pterosin L 3-O-α-L-arabinopyranoside (XI).The structures were elucidated mainly by spectroscopic methods.Compound V was named spelosin.The investigation of two other species, M. calvescens (WALL.) PRESL and M. okamotoi TAGAWA, gave no identifiable compounds, of this type.Keywords--Microlepia speluncae; Microlepia trapeziformis; Microlepia obtusiloba; Microlepia substrigosa; Microlepia strigosa; Microlepia calvescens; Microlepia okamotoi; Pteridaceae; chemotaxonomy; pterosin-type sesquiterpene
