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(1R,4aα,8aα)-Decahydro-1α,4α-naphthalenediol, also known as tetrahydro-1,4-naphthalenediol, is a bicyclic alcohol with the molecular formula C10H18O2. It is a colorless, viscous liquid at room temperature, insoluble in water, and soluble in organic solvents.

1127-51-1

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1127-51-1 Usage

Uses

Used in Pharmaceutical Industry:
(1R,4aα,8aα)-Decahydro-1α,4α-naphthalenediol is used as an intermediate in the production of pharmaceuticals and fine chemicals. It plays a crucial role in the synthesis of various drugs and helps in the development of new therapeutic agents.
Used in Fragrance and Flavoring Industry:
(1R,4aα,8aα)-Decahydro-1α,4α-naphthalenediol is used in the synthesis of fragrances and flavoring agents. Its unique chemical structure contributes to the creation of distinct scents and tastes, enhancing the sensory experience of various products.
Environmental Considerations:
(1R,4aα,8aα)-Decahydro-1α,4α-naphthalenediol has been identified as a potential environmental contaminant and may pose a risk to aquatic organisms. Therefore, proper handling and disposal practices are essential in minimizing its impact on the environment and ensuring the safety of ecosystems.

Check Digit Verification of cas no

The CAS Registry Mumber 1127-51-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1127-51:
(6*1)+(5*1)+(4*2)+(3*7)+(2*5)+(1*1)=51
51 % 10 = 1
So 1127-51-1 is a valid CAS Registry Number.

1127-51-1Relevant academic research and scientific papers

Does substituent's conformation influence the kinetics of reduction reactions on trans-4-X-decal-1-ones and to what extent?

Di Maio, Giorgio,Gabriella Mascia, Maria,Vecchi, Elisabetta

, p. 3313 - 3318 (2007/10/03)

Stereochemistry and relative rates kax and keq of reduction reactions on title compounds have been measured under five different reaction conditions (NaBH4 in i-PrOH, LiBH4 and NaAlH4 in THF and LiAlH4 in THF and in Et2O). Experiments indicate that axial substituents behave as far less electronegative than their equatorial counterpart in reactions at the equatorial side of molecules.

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