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135161-99-8

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135161-99-8 Usage

Class

Anthraquinone

Type

Organic compound

Presence in nature

Commonly found in plants and some insects

Hydroxyl groups

Three hydroxyl groups

Pentyl chain

Attached to the eighth position of the anthraquinone core

Use as a dye and pigment

Vibrant color and ability to bind to materials

Industries

Textiles, ink, and paints

Potential applications

Antioxidant and anti-inflammatory agent

Pharmaceutical and cosmetic applications

Shown potential in these areas

Versatility

Various uses and potential health benefits

Check Digit Verification of cas no

The CAS Registry Mumber 135161-99-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,1,6 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 135161-99:
(8*1)+(7*3)+(6*5)+(5*1)+(4*6)+(3*1)+(2*9)+(1*9)=118
118 % 10 = 8
So 135161-99-8 is a valid CAS Registry Number.
InChI:InChI=1/C19H18O5/c1-2-3-4-5-10-6-11(20)7-13-16(10)19(24)17-14(18(13)23)8-12(21)9-15(17)22/h6-9,20-22H,2-5H2,1H3

135161-99-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,6-trihydroxy-8-pentylanthracene-9,10-dione

1.2 Other means of identification

Product number -
Other names R1128D

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:135161-99-8 SDS

135161-99-8Upstream product

135161-99-8Downstream Products

135161-99-8Relevant articles and documents

Synthesis of non-steroidal estrogen receptor antagonists R1128 A, B, C, and D via an oxazoline-promoted iterative ortho-lithiation strategy

Fukuda, Tsutomu,Fukushima, Koichiro,Sanai, Susumu,Iwao, Masatomo

, p. 133 - 135 (2012/03/07)

A concise total synthesis of non-steroidal estrogen receptor antagonists R1128 A-D (1a-1d) has been achieved using iterative ortho-lithiation of 2-(4-methoxyphenyl)-4,4- dimethyloxazoline (3) as the key reaction.

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