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Decahydronaphthalene-1,4-diol, also known as Decahydro-1,4-dihydroxynaphthalene or Decahydro-1,4-diol, is an organic compound with the chemical formula C10H18O2. It is a cyclic diol, meaning it contains two hydroxyl (-OH) groups attached to a decalin (decahydro-naphthalene) ring structure. decahydronaphthalene-1,4-diol is a colorless liquid with a density of 1.02 g/cm3 and a boiling point of 285°C. It is soluble in water and various organic solvents. Decahydronaphthalene-1,4-diol is primarily used as an intermediate in the synthesis of various chemicals, including pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure and properties make it a valuable building block in the chemical industry.

1127-54-4

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1127-54-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1127-54-4 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 1127-54:
(6*1)+(5*1)+(4*2)+(3*7)+(2*5)+(1*4)=54
54 % 10 = 4
So 1127-54-4 is a valid CAS Registry Number.

1127-54-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,4,4a,5,6,7,8,8a-decahydronaphthalene-1,4-diol

1.2 Other means of identification

Product number -
Other names Decahydro-1,4-naphthalenediol

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:1127-54-4 SDS

1127-54-4Relevant 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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