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49817-16-5

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49817-16-5 Usage

Molecular class

Alcohols

Backbone structure

2,4-pentadienol

Substitution

3-methyl-5-(2,6,6-trimethyl-1-cyclohexen-1-yl)

Stereochemistry

(4E)-stereoisomeric form, indicating a trans configuration of the double bond

Potential applications

Organic synthesis, pharmaceuticals, and fragrance industry due to unique structure and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 49817-16-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,8,1 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 49817-16:
(7*4)+(6*9)+(5*8)+(4*1)+(3*7)+(2*1)+(1*6)=155
155 % 10 = 5
So 49817-16-5 is a valid CAS Registry Number.

49817-16-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name β-apo-12-carotenol

1.2 Other means of identification

Product number -
Other names β-Ionyliden-ethanol

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:49817-16-5 SDS

49817-16-5Relevant articles and documents

Synthesis of isotopically labeled all-trans retinals for DNP-enhanced solid-state NMR studies of retinylidene proteins

Leeder, Alexander J.,Brown, Lynda J.,Becker-Baldus, Johanna,Mehler, Michaela,Glaubitz, Clemens,Brown, Richard C.D.

, (2018/02/06)

Three all-trans retinals containing multiple 13C labels have been synthesized to enable dynamic nuclear polarization enhanced solid-state magic angle spinning NMR studies of novel microbial retinylidene membrane proteins including proteorhodpsi

Animal carotenoids. 8. Synthesis of beta, gamma-carotene and gamma, gamma-carotene.

Andrewes,Liaaen-Jensen

, p. 1401 - 1409 (2007/10/12)

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