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161894-77-5

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161894-77-5 Usage

Physical state

Colorless liquid

Explanation

Different sources of media describe the Explanation of 161894-77-5 differently. You can refer to the following data:
1. The compound is in a liquid state and has no color.
2. The compound has a noticeable and intense smell that can be easily detected.
3. Due to its strong and pungent odor, this compound is used as a component in the fragrance industry, specifically in the production of perfumes and other cosmetic products.
4. The compound serves as a starting material or intermediate in the chemical reactions that produce other organic compounds.
5. 1,3-Dioxane-4-carboxaldehyde, 2,2,6-trimethyl-, trans(9CI) can cause irritation upon contact with skin, eyes, or respiratory system.

Odor

Strong, pungent

Application

Fragrance ingredient in perfumes and cosmetic products

Synthesis

Used in the synthesis of various organic compounds

Safety

Potential irritant

Check Digit Verification of cas no

The CAS Registry Mumber 161894-77-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,8,9 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 161894-77:
(8*1)+(7*6)+(6*1)+(5*8)+(4*9)+(3*4)+(2*7)+(1*7)=165
165 % 10 = 5
So 161894-77-5 is a valid CAS Registry Number.

161894-77-5Downstream Products

161894-77-5Relevant articles and documents

Enzymatic approach to enantiomerically pure 5-alken-2,4-diols and 4-hydroxy-5-alken-2-ones: Application to the synthesis of chiral synthons

Abate, Agnese,Brenna, Elisabetta,Costantini, Alessia,Fuganti, Claudio,Gatti, Francesco G.,Malpezzi, Luciana,Serra, Stefano

, p. 5228 - 5240 (2007/10/03)

Enantiomerically pure 1,3-diols 1-3 were obtained by a chemoenzymatic approach (lipase PS from Burkholderia cepacia). These diols were converted into useful chiral synthons, which could be considered homologues of glyceraldehyde and glyceric acid acetonid

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