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cis-1,2,3,4-Tetrahydro-5-(oxiranylmethoxy)-2,3-naphthalenediol is an organic chemical compound that is primarily found in scientific research and experimentation. It features an oxiranyl group, also known as an epoxide group, attached via a methoxy linkage to a naphthalene core. This core is further modified by the addition of two hydroxyl groups and the conversion to a tetrahydronaphthalene structure. cis-1,2,3,4-Tetrahydro-5-(oxiranylmethoxy)-2,3-naphthalenediol's exact molecular structure and properties are determined by this combination of various functional groups. However, detailed information regarding its properties, uses, or potential applications is not readily available, suggesting that it may be a specialized or less commonly used chemical.

35697-15-5

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35697-15-5 Usage

Uses

Due to the lack of specific information on the uses of cis-1,2,3,4-Tetrahydro-5-(oxiranylmethoxy)-2,3-naphthalenediol, it is not possible to provide a detailed list of applications. However, given its presence in scientific research and experimentation, it can be inferred that cis-1,2,3,4-Tetrahydro-5-(oxiranylmethoxy)-2,3-naphthalenediol may be used in various research applications, such as:
Used in Scientific Research:
cis-1,2,3,4-Tetrahydro-5-(oxiranylmethoxy)-2,3-naphthalenediol is used as a research chemical for [application type] due to its unique molecular structure and potential for [application reason].
Used in Pharmaceutical Development:
cis-1,2,3,4-Tetrahydro-5-(oxiranylmethoxy)-2,3-naphthalenediol is used as a potential pharmaceutical candidate for [application type] because of its [application reason].

Check Digit Verification of cas no

The CAS Registry Mumber 35697-15-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,6,9 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 35697-15:
(7*3)+(6*5)+(5*6)+(4*9)+(3*7)+(2*1)+(1*5)=145
145 % 10 = 5
So 35697-15-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H16O4/c14-11-4-8-2-1-3-13(10(8)5-12(11)15)17-7-9-6-16-9/h1-3,9,11-12,14-15H,4-7H2/t9?,11-,12+/m0/s1

35697-15-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,3S)-5-(oxiran-2-ylmethoxy)-1,2,3,4-tetrahydronaphthalene-2,3-diol

1.2 Other means of identification

Product number -
Other names 5-oxiranylmethoxy-1,2,3,4-tetrahydro-naphthalene-2,3-diol

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:35697-15-5 SDS

35697-15-5Upstream product

35697-15-5Downstream Products

35697-15-5Relevant academic research and scientific papers

Nondepressant β-adrenergic blocking agents. I Substituted 3-amino-1-(5, 6, 7, 8-tetrahydro-1-naphthoxy)-2-propanols

Condon,Cimarusti,Fox,Narayanan,Reid,Sundeen,Hauck

, p. 913 - 922 (2007/10/06)

A series of 3-amino-1-(5,6,7,8-tetrahydronaphthoxy)-2-propanols was synthesized and investigated for β-adrenergic blocking activity and direct myocardial depressant action. The cis- and trans-diols 12-15 were found to retain the β-blocking potency of propranolol but to lack its myocardial depressant action. Compound 15 (nadolol) is currently undergoing extensive clinical evaluation as a potential antianginal, antiarrhythmic, and antihypertensive agent.

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