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16849-44-8

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  • 6H-Dibenzo[b,d]pyran-1-ol,6a,7,8,9,10,10a-hexahydro-6,6-dimethyl-9-methylene-3-pentyl-, trans- (8CI,9CI)

    Cas No: 16849-44-8

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16849-44-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16849-44-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,4 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16849-44:
(7*1)+(6*6)+(5*8)+(4*4)+(3*9)+(2*4)+(1*4)=138
138 % 10 = 8
So 16849-44-8 is a valid CAS Registry Number.
InChI:InChI=1/C21H30O2/c1-5-6-7-8-15-12-18(22)20-16-11-14(2)9-10-17(16)21(3,4)23-19(20)13-15/h12-13,16-17,22H,2,5-11H2,1,3-4H3/t16-,17-/m1/s1

16849-44-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (6aR,10aR)-6,6-dimethyl-9-methylidene-3-pentyl-7,8,10,10a-tetrahydro-6aH-benzo[c]chromen-1-ol

1.2 Other means of identification

Product number -
Other names (6ar,10ar)-6,6-dimethyl-9-methylidene-3-pentyl-6a,7,8,9,10,10a-hexahydro-6h-benzo[c]chromen-1-ol

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:16849-44-8 SDS

16849-44-8Downstream Products

16849-44-8Relevant articles and documents

Novel synthesis of (-)-trans-Δ9,11-tetrahydrocannabinol

Banijamali,Makriyannis

, p. 823 - 825 (2007/10/02)

Addition of hydrogen chloride gas to a solution of Δ8-tetrahydrocannabinol in dry dichloromethane at -60° in the presence of zinc chloride results in the formation of a higher concentration of 9-α-chlorohexahydrocannabinol (75%) than the thermodynamically more stable 9-β-chlorohexahydrocannabinol (25%). The two isomers can be separated by reverse-phase hplc. Elimination of hydrogen chloride from 9-α-chlorohexahydrocannabinol using potassium t-amylate under anhydrous conditions gives exclusively Δ9,11-tetrahydrocannabinol in overall yield of 65%.

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