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11-hydroxymethylbenzo(a)pyrene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

94500-53-5

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94500-53-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94500-53-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,5,0 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 94500-53:
(7*9)+(6*4)+(5*5)+(4*0)+(3*0)+(2*5)+(1*3)=125
125 % 10 = 5
So 94500-53-5 is a valid CAS Registry Number.
InChI:InChI=1/C21H14O/c22-12-17-11-15-6-3-5-13-8-9-16-10-14-4-1-2-7-18(14)20(17)21(16)19(13)15/h1-11,22H,12H2

94500-53-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name benzo[a]pyren-11-ylmethanol

1.2 Other means of identification

Product number -
Other names -

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:94500-53-5 SDS

94500-53-5Downstream Products

94500-53-5Relevant academic research and scientific papers

Synthesis of 4-, 5-, 11-, and 12-(Chloromethyl)benzopyrene

Leon, Alberto A.,Daub, Guido H.,VanderJagt, David L.

, p. 553 - 556 (1985)

The previously unknown title compounds have been synthesized in excellent yields from the ethyl arylacetates 3a-d.Formylation of 3a-d allowed the isolation of formyl esters 4a-d that were cyclized by a novel procedure utilizing dilute solutions (5-10percent) of methanesulfonic acid in methylene chloride.The resulting benzopyrene ethyl esters were transformed to the target chloromethyl compound by reduction (LAH) followed by reaction with thionyl chloride.The overall yields obtained from esters 3a-d ranged from 44percent to 66percent.These compounds can be used as immediate precursors of benzopyrenylmethyl carbocations which are believed to be relevant in certain carcinogenesis mechanisms.

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